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TORREYA 


A Montuty Journat or Botanicat Nores anp News 


JOHN TORREY, 1796-1873 


LIRRABY 
Bera 
GA (ist 


EDITED FOR 
THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


Volume XIX 


NEW YORK 
Zoe 9 


vale , ‘ PRESS OF at 
Tg af | THE NEW ERA PRINTING COMPANY ‘f 
, Pas haa a, LANCASTER, PA. 


THE TORREY BOTANICAL CLUB 


OFFICERS FOR 


1919 


President 
H. M. RICHARDS, Sc.D. 


Vice- Presidents. 
JOHN HENDLEY BARNHART, A.M., M.D 
C. STUART GAGER, PH.D. 


Secretary and Treasurer 
BERNARD O. DODGE, Pu.D. 
COLUMBIA UNIVERSITY, N. Y. City. 


Editor 


ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


JEAN BROADHURST, Pu.D. 
J. A. HARRIS, Px.D. 


MARSHALL AVERY HOWE, Pu.D. 


M. LEVINE, Pu.D. 
G. E. NICHOLS, Pu.D. 
ARLOW B. STOUT, Pu.D. 


NORMAN TAYLOR. 


Delegate to the Council of the New York Academy of Sciences 
M. A. HOWE, PH.D. 


Committees for 1919. 


Finance Committee 


R. A. HARPER, Chairman. 
J. H. BARNHART, 

Miss C. C. HAYNES 
SERENO STETSON 


Budget Committee 


J. H. BARNHART, Chairman. 
R. A. HARPER 

N. L. BRITTON 

A. W. EVANS 

M. A. Howe 

H. H. Russy 


Field Committee 


F. W. PENNELL, Chairman. 
Mrs. L. M. KEELER 
MICHAEL LEVINE 

GEORGE T. HASTINGS 
Percy WILSON 

F. J. SEAVER 


Program Committee 


Mrs. E.G. BRITTON, Chairman. 
Pror. JEAN BROADHURST 

B. O. DODGE 

MICHAEL LEVINE 

F. J. SEAVER 


Membership Committee 
J. K. SMALL, Chairman. 
T. E. HAZEN 
E. W. OLIVE 
Local Flora Committee 
N. L. Britton, Chairman. 


Phanerogams: Cryptogams: 
E. P. BICKNELL Mrs. E.G. BRITTON 
N. L. BRITTON T. E. HAZEN 
CS €. Curzis M. A. Howe 


K. K. MACKENZIE MICHAEL LEVINE 
NORMAN TAYLOR W. A. MuRRILL 


Chairmen of Special Committees on Local Flora 


Ferns and Fern Allies: R. C. Benedict. 


Mosses: Mrs. E. G. Britton 
Liverworts: A. W. Evans 

Fresh Water Algae: T. E. Hazen 
Marine Algae: M. A. Howe 
Gasteromycetes: G. C. Fisher 
Hymeroomycetes: W. A. Murrill 


Except Russulaand Lactarius: Miss G. 


Burlingham 
Cortinarius: R. A. Harper 
Polyporeae: M. Levine 
Exobasidii: H. M. Richards 
Rusts and Smuts: E. W. Olive 
Discomycetes: B. O. Dodge 


Lichens: W. C. Barbour 


Sphaeriaceae, Dothideaceae: H. M. 
Richards 
Hypocreaceae, Perisporieae, Plectas- 


cineae, Tuberineae: F. J. Seaver 

Fungi-forming sclerotia: A. B. Stout 
Imperfecti: H. M. Richards, F. 

Seaver, Mel T. Cook 
Oomycetes: C. A. King 
Zygomycetes: A. F. Blakeslee 
Chytridiaceae, 
Myxomycetes: Mrs. H. M. Richards 
Yeast and Bacteria: Prof. J. Broadhurst 
Insect galls: Mel T. Cook 


Vol. 19 January, IgI9g No. 1 


PeLORREYA 


A Monruiy Journat or BoranicaL Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 
BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873. 
CONTENTS 
The Pala or Mule’s Foot Fetn in the Hawaiian Archipelago: VaucHan Mac- 
AOANIG ETESY oc) sosdaset dv ddocdvessieacnumra ged PoVONY Los Scape Faae toe cwons ctupaleimdiobe ste ak soda teas I 
Pleistocene Plants from Tennessee and Mississippi: E. W. BERRY..0......c.-esseee ees 8 
Nates-on Ly castes. Ty Dy Al. COCKEREEL$ oi nce acy bes op shoe siveseln ch b chenedrntens sompheiwenecy heb Io 
Shorter notes: 
Plants in flower in the Autumn of 1918 on Long Island, N. Y.: W. C. Frr- 
MUSON > on oes oc aicc cp vine necesuce Vocpoe oianeie sonsaealer apdusicbebecedeeedniniee Msp rinactiepos dee scar velde tiene 1z 
Concerning duplicate types: F. W. PENNELL........64.. Peasy Wee Ae 0 ton Sa heheate I4 
Reviews; 
Boerker’s Our National Forests: C, STUART GAGER.....sssecensesecn cee estesesnecseres 14 
_Harwood’s New Creations in Plant Life: O. BE. WHITE...-..06. 000.00 ccseee geese eeee 16 
Proceedings of the Club ..........ccc000 ceececaueceeereees Pi erarmus natok deny Chak wld a Pa 17 
BR MEIPA LEIA). SL ih 502i gow sc as co cUe Mess Ria hobs No dcaccanOPer vane tev aidenided Wuepae cea dpasekinneed 19 
Y PUBLISHED FOR THE CLUB 


At 41 NortH Queen Srreetr, LANcCAsrER, Pa. 
“x BY THe New Era Printing Company 
“Entered at the Post Office at Lancaster, Pa,, as second-class matter, 


THE TORREY BOTANICAL CLUB 


OFFICERS FOR to19 


President 
H. M. RICHARDS, Sc.D. 


_ Vice- Presidents. 
JOHN HENDLEY BARNHART, A.M., M.D 
C. STUART GAGER, PH.D. 


_ Secretary and Treasurer 
BERNARD O. DODGE, PH.D. 
COLUMBIA UNIveErRsiItTy, N. Y. City. 
_ Editor 
ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


JEAN BROADHURST, Pu.D. : M. LEVINE, Pu.D. 
J. A. HARRIS, Px.D. G.. E. NICHOLS, Px.D. 


~MARSHALL AVERY HOWE, Pu.D. -ARLOW B. STOUT, PH.D. 
NORMAN TAYLOR. 


Delegate io the Council of the New York Academy of Sciences | 
: M. A. HOWE, PH.D. 


OFFICIAL ORGAN OF THE WILD FLOWER PRESERVATION ~ 


SociETY oF AMERICA 


TORREYA is furnished to subscribers in the United States and 
Canada for one dollar per annum; single copies, fifteen cents. To 
subscribers elsewhere, five shillings, or the equivalent thereof. Postal or 
express money orders and drafts or personal checks on New York City 
banks are accepted in payment, but the rules of the New York Clearing 
House compel the request that ten cents be added to the amount of any 
other local checks that may be sent. Subscriptions are received only 
for full volumes, beginning with the January issue. Reprints will be 
furnished at cost prices. Subscriptions and remittances should be sent 
to TREASURER, TORREY BOTANICAL CLus, 41 North Queen St., Lan- 
caster, Pa., or Columbia University, New York City. 

Matter for publication, and books and papers for review, should 
be addressed to i 


NORMAN TAYLOR 


‘Brooklyn Botanic Garden 
Brooklyn, N. Y 


TORREYA 


Vol. I9 No. 1 
January, IgI9 


THE PALA OR MULE’S-FOOT FERN (Marattia Doug- 
lasvi (Presl.) Baker) IN THE HAWAIIAN 
ARCHIPELAGO 


By VauGHAN MAcCCAUGHEY 


College of Hawaii, Honolulu, Hawaii 


The Hawaiian ferns have constituted an interesting subject 
of botanical investigation for over a century. There have been 
few studies, however, of specific ferns or fern groups.1 The 
present paper aims to give a concise account of the “‘mule’s-foot”’ 
fern or pala (Marattia Douglasii (Presl.) Baker). This species 
is of particular interest because it is the sole representative, in 
the present Hawaiian flora, of an extremely important group of 
pteridophytes, namely, the Marattiales. Moreover, it also oc- 
curs in the Fiji Islands, and this fact raises some interesting ques- 
tions as to its geographic dissemination. The pala was also used 
as food and medicine by the primitive Hawaiians. Finally, 
Campbell’s? studies of the gametophyte stage have given local 
workers a special interest in this fern. 

In early geologic periods Marattiaceous ferns abounded, and 
comprised an important element in the luxuriant fern jungles of 
those times. They were very abundant in the Pennsylvanian 
(Upper Carboniferous), in the Triassic (Rhetic), and in the Meso- 
zoic of India. A survey of the geological record shows that the 
present-day Marattiales are but scant and skrunken remnants 
of a magnificent vanished flora. 

The ancient and primitive family Marattiaceae is represented 


1MacCaughey, V. Genus Gleichenia in the Hawaiian Islands. Torreya 18: 
41-52. 1918. 

2 Campbell, D. H. Observations on the development of Marattia douglasit 
Baker. Ann. Bot. 8:1. 18094. 
(No. 12, Vol. 18 of ToRREYA, comprising pp. 231-258, was issued 21 January 1919) 


1 


Ltr 4, 
NB Ww Ye 


GARD; 


2 


in the Hawaiian flora only by a single species, M. Douglasii. 
The geographic range of the family i: .dicated by the following 
table: 


Genus No. of species Range 
Marattia 25 tropics 
Angiopteris I (or 60!) Old World tropics, Australasia, S. Japan 
Archangiopteris I southwestern China 
Kaulfussia I Indo-Malaya, Philippines 
Macroglossum I Borneo 
Danaea 20 Tropical America 


From this table will be seen that Hawaii, isolated in the vast 
stretches of the North Pacific_Ocean, and lying on the rim of the 
tropics, is the northernmost limit of the family’s range in the 
entire Pacific basin. 

Three theories may be presented to explain the occurrence of 
M. Douglasii in the Hawaiian Islands. First: It also occurs in 
the Fiji Archipelago. Inasmuch as the bulk of the native Ha- 
walian flora shows affinities with that of the southwest Pacific, 
it is possible that the pala was introduced through natural agen- 
cies,—ex. wind,—from the South Pacific. Second: The native 
Hawaiians habitually used the pala for food and medicine. The 
natives originally migrated to Hawaii from Tahiti, and for many 
centuries maintained intercourse with their southern kinsfolk. 
During this period of migration and intercourse, numerous food 
plants' were introduced into Hawaii. It is not at all unlikely 
that the pala was deliberately introduced, by the natives, during 
this epoch. Its present distribution in the is!ands is in no way 
incompatible with this hypothesis. 

Third: The entire Hawaiian Archipelago has undergone pro- 
found subsidence during recent geologic time.2 In early times 
the islands were united by land connections. This formed a 
“Pan-Hawaii-land,’”’ very much larger in area, higher in eleva- 
tion, and diversified in topography and climate, than the present 
archipelago. On the warm lowlands of Pan-Hawaii-land may 
have existed great tropical jungles of Marattiaceous ferns and 


1 MacCaughey, V. Food Plants of the Ancient Hawaiians. Sci. Monthly 4: 
75-80. I917. 

2 MacCaughey, V. Outstanding Biological Features of the Hawaiian Archi- 
pelago. Amer. Nat. in press. 


their allies. All have vanished save the lone M. Douglasii, that 
was able to survive under the changing ecologic environment. 
There is ample evidence elsewhere in the Hawaiian flora to show 
that many elements of the present flora are but remnants of the 
far richer flora of Pan-Hawaii-land. 

The genus Marattia Sm. (—Dicostegia Presl., Eupodium J.Sm., 
Gymnotheca Presl., Marattia Presl., Myriotheca Bory, Stibasia 
Presl.) was named in honor of an Italian botanist, J. F. Maratti, 
of Vallombrosa, Tuscany, who lived in the seventeenth century 
and wrote on ferns. The genus comprises about 25 species, 
which are scattered throughout the tropics, and into the southern 
hemisphere. The following table shows the distribution of the 
better-known species. 

O_p WorLD 
African 
fraxinea Sm.—west coast of Africa to Polynesia. 
salicifolia Schrad.—South Africa to the Cape. 
Boivini Mett.—Madagascar. 
purpurascens de Vriese—Ascencion Island. 


East Indies 


salicina Sm.—East Indian Archipelago. 
sambucina Bl.—Java. 
pellucida Pres|.—Philippine Islands. 


Melanesia 


melanesiaca Kuhn—Melanesia. 
attenuata Labill—New Caledonia. 


Polynesia 


Douglasii (Presl.) Baker—Fiji, Hawaiian Islands. 


NEw Wor.LpD 
cicutifolia Kaulf.—tropical America. 
Kaulfussii J. Sm.—tropical America. 
alata Sm.—West Indies, Mexico, northern South America. 
Weinmannitfolia. Liebm.—Mexico. 
laevis Sm.—West Indies. 


= 


Marattia Douglasii (Presl.) Baker! is called pala by the Ha- 
walians. It may also be called the Mule’s-foot Fern, or Doug- 
las’s Marattia. It was named in honor of the Scotch botanist, 
David Douglas, who visited Hawaii in 1833, and lost his life by 
falling into a native cattle-trap. 

It is a large, coarse-leaved, showy fern, easily recognized in 
the forest. Although not as large as the Marattias of other 
countries, it attains generous size, with a stocky trunk 1-2 it. 
high, and wide-spreading leaves, 6-15 ft. long. “In Hawaii Ma- 
rattia is surpassed in stature and spread by some of the arbor- 
escent species (Cibotium, Sadleria”). Aside from the strictly 
arborescent species, however, Marattia and Angiopteris may be 
ranked among the largest of the ferns. 

The pala is abundant in the mountain-forests of Hawaii, and 
in the moister parts of the lower forests. It inhabits the humid 
zone lying between 800-3500 ft., on both windward and leeward 
slopes. It favorite haunts are cool, heavily shaded, humid, steep- 
sloped ravines, where it forms little colonies or patches. It 
seems to prefer sharply sloping banks and ravine-sides, although 
it is also found in level places. The pala is strongly hygrophytic 
and shade-loving; it is never found in dry or exposed situations. 

Representative regions where the pala is abundant are: 
Hanalei and Na Pali districts, Kauai; Kaala and Punaluu dis- 
tricts, Oahu; valleys of northeastern Molokai; mountains back 
of Lahaina and Wailuku, Maui; forests of windward Haleakala, 
Maui; forests of Hilo, Hamakua, Olaa, and Kona, Hawaii. 
There are no places where it is excessively abundant; it is scat- 
tered rather sparingly through the forests and groves. 

The stem or trunk is tuberous, barrel-shaped, or almost glob- 
ular. It is stocky and erect, as is also true of Angiopteris. 
Danea and Kaulfussia have more or less horizontal rhizomes. 
The pala stem is sometimes half buried under leafmould and earth, 
but on the steeper slopes, where the pala best luxuriates, it is 
almost wholly exposed. 


1W. J. Hooker and J. G. Baker. Synopsis Filicum. London, 1868, p. 441. 
Also called Stibasia Douglasii Presl., Gymnotheca Douglasii T. Moore, M. alata 
Hook. & Arn. 

2 MacCaughey, V. Tree Ferns of Hawaii. American Botanist, 22: 1-9. 10916. 


i) 

The stem is completely covered by the conspicuous, dark, 
fleshy auricles (stipules) and leaf-bases. The petioles arise from 
among the brownish or purplish auricles. After the fall of the 
leaf the fleshy base remains alive and often gives rise to adven- 
titious buds. Hooker, in describing the stipules of MW. purpur- 
ascens De Vriese states that they may become ‘“‘leafy at the mar- 
gin, lobed and crestd, green, sometimes even becoming sorif- 
erous pinnules.’’ The leaf-bases of the pala have been well de- 
scribed by Camptell :! 

“The leaves are furnished at the base with very conspicuous 
fleshy stipules which remain adhering to the stem after the leaf 
has fallen away, and these leaf-bases, with their attached stip- 
ules, more or less completely cover the surface of the stem. As 
the leaves fall away they leave a characteristic scar marked by 
the remains of the vascular bundles. The leaf-base as well as 
the stalks of the leaflets show a more or less marked enlarge- 
ment, recalling the pulvinus which occurs so commonly in the 
Leguminosae. It is at this point that the leaf-stalk separates, 
the smaller divisions of the leaf often breaking away from the 
main or secondary rachis, in the same fashion as the main leaf- 
stalk falls. In the large species of Marattia and Angiopteris 
this enlarged leaf-base with the two thick, fleshy stipules curi- 
ously resembles in shape and size the hoof of a horse.” 

The present writer would suggest that the comparison with a 
mule’s hoof would be more apt, and proposes as the common 
name, ‘“‘MULE’S-FOOT’’ FERN. 

The thick, fleshy auricles are richly supplied with starch and 
mucilage, and were used by the primitive Hawaiians as an article 
of food, when other food supplies were lacking. The ‘‘mule’s 
feet’’ were baked in hot ashes, whereupon they became very pal- 
atable. The writer has frequently eaten baked pala, and can 
testify to its excellence. The pala stipules were also used med- 
icinally, for bronchial and intestinal catarrh. Slices soaked in 
cold water soon impart their mucilage to the liquid, and form a 
pleasant drink. 

In cross section the starchy, watery stem shows a complicated 
system of steles, arranged in concentric circles. Sclerenchyma 
is absent from its ground tissue. 

1). H. Campbell. The Eusporangiatae, 1911, p. 118. 


6 


The pala roots are short, thick, and fleshy. They originate 
with reference to the stele circles in the stem. The central cyl- 
inder of the root has several alternating groups of xylem and 
phloem. Tannin sacs are abundantly developed in the roots, 
as well as in other parts of the plant. 

The pala foliage is stately and somber. The leaves are few in 
number (5-150), spirally arranged, and with close-set bases. 
The young leaves are enclosed in the prominent stipules; the 
leaves are circinate, and slowly unfurl in the typical fern manner. 
The leaves develop very slowly,—a period of 3 to 6 months being 
required for the unfurling of a single leaf. Indeed, all of the 
vital functions of the pala, like those of other rain forest plants, 
are very sluggish. 

The petioles are 3 to 5 feet long, stout, smooth, and shining. 
At the base they are conspicuously swollen, articulate, and 2.5-3 
ins. in diameter. The ‘‘mule’s-foot’’ base, with its two large, 
fleshy, auricular stipules, has already been described. Lenticel- 
like structures are of common occurrence on the older leaf-bases. 
They arise beneath the stomata, and form small cavities, the 
peripheral cells of which become detached and dried up. Large 
mucilage ducts and numerous tannin sacs are developed in the 
petioles of the older leaves. 

The leaf-blade is 3 to 8 ft. long, deltoid or ovate-oblong, and 
2-3-pinnate. The base is 3-pinnate; there is a terminal pinnule. 
The blade is a characteristic dark green, smooth, glossy, and not- 
ably fleshy. The color and texture are quite distinctive. A 
cross-section of leaf reveals a thick layer of collenchymous 
hypodermal tissue. 

The pinnae are oblong-lanceolate. The lowest pinnae are 6— 
24 in. long, on stalks of .5-2.5 in. The upper portion of the 
rachis is narrowly margined or winged. The secondary pinnae 
are linear, 3-6 in. long, with a broadly compressed or winged 
rachis. The ultimate pinnules are substipitate, ovate or ob- 
long, .5—I ins. long by .25-.30 in. wide, and bluntly serrate. The 
apex is obtuse or acuminate; the base is cuneate or subtruncate. 
The veins are simple or dichotomously forked. 

All the leaves are spore-beaiing or potentially so. The spor- 


~I 


angia are large, fleshy, and borne in boat-shaped groups (syn- 
angia), on the under surface of the pinnule, near the margin. 
The sporangia, each of which arises from a number of superficial 
cells, are incompletely separated from one another, and remain 
together in the oblong or capsule-like synangia. The walls of the 
sporangium are several cells in thickness. The annulus is want- 
ing or greatly reduced; there is no indusium. The synangium 
is adnate to the vein, or very short-stalked. Dehiscence is first 
by the opening of the synangial valve, then slits along each 
sporangium. 

Campbell' has made detailed studies of the gametophyte. 
The spores are very small, bilateral or tetrahedral, and yellow- 
ish-brown. Under suitable conditions they germinate promptly. 
Within a week they begin to show a greenish tint, due to the 
developing chlorophyll. The mature gametophyte is large, 
fleshy, massive, dark-green, and heart-shaped. It grows on the 
surface of the soil and closely resembles such liverworts as Pellia. 
It is broad heart-shaped, tapering to a narrow base. The very 
old gametophytes branch dichotomously exactly as in the thal- 
lose liverworts. ‘‘A broad midrib extends for nearly the whole 
length of the thallus and merges gradually into the wings, which 


’ 


are also several-layered, nearly or quite to the margin’’—Camp- 
bell. Rhizoids,—brown, unicellular, and thin-walled,—are pro- 
duced abundantly from the cells of the lower surface. 

The gametophyte is monoecious. Antheridia appear first, 
sometimes on the upper surface, but usually along the lower side 
of the midrib. The archegonia are confined exclusively to the 
lower surface of the midrib. Campbell points out that the re- 
productive organs are very much like those of Ophioglossum, and 
are ‘‘marked indications of the primitive nature of these ancient. 
ferns.”’ 

The Marattia gametophyte is always infested with a specific 
endophytic fungus. Campbell states that it is probably iden- 
tical with or very closely related to the fungus which occurs in 
Ophioglossum. ‘‘In the infested cells of the green gametophyte 
the starch and chromatophores are destroyed by the action of 


1[—). H. Campbell. The Eusporangiatae, 1911. Mosses and Ferns, 1905. 


8 


the endophyte, but the nucleus of the cell remains intact.’ The 
duration of the gametophyte is apparently unlimited, so long as 
fertilization does not take place. The young sporophyte con- 
sists at first mainly of the primary leaf and root, which are tra- 
versed by a single axial vascular strand. A stem apex is de- 
veloped at an early period, although it remains relatively incon- 
spicuous. 

The pala does not occur in cultivation, to the writer’s knowl- 
edge. It undoubtedly would grow successfully under humid 
fern-house conditions, as do many other Hawaiian ferns. M. 
fraxinea Smith, which ranges from west Africa to New Zealand, 
is cultivated in American conservatories. The Hawaiian pala 
would likewise give a magnificent tropical effect in northern 
greenhouses. It deserves attention. 


PLEISTOCENE PLANTS FROM TENNESSEE AND 
MISSISSIPPI 


By Epwarp W. BERRY 


I have published, from time to time, brief accounts of Pleisto- 
cene plants from our Atlantic and Gulf states as they have passed 
through my hands, since the amount of material likely to be 
available does not warrant a more comprehensive treatment. 
For this reason I wish to place on record the following new oc- 
currences. 

It is to be hoped that the distribution of our floras in the era 
immediately preceding the present be considered by botanists 
dealing with the existing flora. Even in the present unsatis- 
-factory state of our knowledge of Pleistocene plants, woefully 
behind that of other civilized countries, much is to be gained in 
insight and many pitfalls may be avoided by looking back of the 
present. 

This note relates to small collections made by Bruce Wade 
in 1915 at Adamsville, McNairy County, Tennessee, from 
next to the highest terrace of the Tennessee River (elevation 
about 500 ft.), and by E. W. Shaw from the Loess just west of 


9 


Vicksburg Military Park, Warren County, Mississippi (the Bluff 
formation of Hilgard). 

The number of species in these two collections is small and 
the forms are not especially noteworthy in that they do not 
occur outside the existing range of the formsinvolved. The hack- 
berry (Celtis mississippiensis) is recorded for the first time from 
the Pleistocene; Lesquereux’s old determination of the chin- 
quapin from the banks of the Mississippi River is in a measure 
corroborated by finding it fossil in western Tennessee; and the 
range of the Pleistocene ancestor of the spanish oak is consider- 
ably extended. Following are the species recognized with brief 
annotations: 

OSMUNDA (?) sp. 

Based upon rootstocks collected by Mr. Wade at Adamsville. 
Similar remains, likewise referred to Osmunda, were described 
by Hollick'! from the late Pleistocene (Talbot formation) of 
Maryland, and the foliage of Osmunda spectabilis Willd. occurs 
in the Pleistocene of Alabama.” 


QUERCUS PREDIGITATA Berry. 

This form, the supposed ancestral type of the existing Quercus 
digitata and Quercus pagodaefolia, has been recorded previously 
from the Pleistocene of North Carolina,*? Mississippi,* and Vir- 
ginia.® It is represented at Adamsville by leaves, cupules and 
acorns, thus considerably extending its known range. 


CASTANEA PUMILA Miller. 

The small chestnut or chinquapin has been recorded by 
Knowlton® from the Pleistocene near Morgantown, West Vir- 
ginia, and by Lesquereux’ from the early Pleistocene near Co- 
lumbus, Kentucky. Although I have collected materials from 
Lesquereux’s locality and adjacent outcrops* I did not meet 

1 Hollick, A. Md. Geol. Surv. Pleist. 217. pl. 67. f. 3. 1906. 

2 Berry, E.W. Am. Jour. Sci. 29: 391. IgI0. 

3 Berry, E.W. Jour. Geol. 15: 342. 1907. 

4 Berry, E.W. Torreya 14: 162. 1914. 

5 Berry, E.W. Am. Jour. ‘Sci. 34: 22. f. 4, 5. 1912. 

® Knowlton, F. H. Am. Geol. 18: 371. 1896. 

*Lesquereux, L. Am. Jour. Sci. 27: 365. 1850. 

8 Berry, E. W. Proc. U. S. Nat. Mus. 48: 293-303. pls. 12, 13. I915. 


10 


with this species. Nevertheless I see no reason for doubting 
Lesquereux’s determination beyond the fact that he queried it. 
The present occurrence is based upon characteristic nuts collected 
by Mr. Wade at Adamsville. 

CELTIS MISSISSIPPIENSIS Bosc. 

This species, so far as I know, has not previously been found 
fossil. The present occurrence is based upon beautifully pre- 
served, reticulate surfaced stones collected from the Loess at 
Vicksburg, Mississippi, by E. W. Shaw at a horizon 10 feet be- 
low the surface. The related Celtis occidentalis Linné is repre- 
sented by stones in the late Pleistocene (Talbot formation) at 
Tappahannock, Virginia.! 


THE JOHNS HOPKINS UNIVERSITY. 


NORES) ONVEY GASTE 
By T. D. A. COCKERELL 


Among the various neotropical orchids, few are more attrac- 
tive than the species of Lycaste. Several years ago Mrs. Cock- 
erell brought three forms from Guatemala, and we have had 
abundant opportunity to study their characters, as they flowered 
each season in the greenhouse. The plants were purchased in 
Guatemala City, but were brought from the surrounding coun- 
try by the natives. The most. interesting and beautiful is the. 
one known in horticulture as Lycaste Skinnert var. alba. After 
comparing the living plants with typical L. Skinnert, flowering at 
the same time, I came to the conclusion that the so-called var- 
iety alba was a distinct species. It apparently occurs wild, and 
in spite of assertions to the contrary, it certainly has structural 
as well as color characters. The lateral lobes of the lower petal 
or lip are much larger in Skinneri than in alba; while the bract 
of Skinneri is much shorter, not reaching the middle of the upper 
sepal. I wrote to Mr. R. A. Rolfe concerning the matter, and 
he discussed the question briefly in Orchid Review, 1915, p. 224. 
He did not believe that alba could be a distinct species, and I 

1 Berry, E. W. Am. Nat. 43: 435. 1909. 


11 


hesitated to combat his opinion, although he presented no de 
cisive evidence. As no more light has come to clear up the mat- 
ter, and it still seems to me at least probable that the white form 
should be separated, I offer a brief description from our material. 


et LycastTE alba sp. nov. 


Scapes light green, 4.25 mm. thick; posterior bract sheathing, 
the sides infolding, so that the long apical part is hollow, apex 
tapering, sharply pointed, base 10.5 mm. wide, the back very 
obtusely keeled, length of bract about 72 mm., light green; an- 
terior bract represented by a small projection about 2 mm. long, 
pointed with a membranous appendage; sepals pure white, upper 
erect, about 75 mm. long and 36 broad, lanceolate ovate, obtusely 
pointed, keeled beneath apically; lateral sepals similar, faintly 
greenish apically beneath, about 77 mm. long and 38 broad, 
meeting below and slightly overlapping to form a gibbous chin; 
the upper sepal goes 24 mm. beyond tip of bract; petals pure 
white, the lower one (lip) suffused with orange at extreme base; 
lateral petals about 50 mm. long and 30 broad, the broad apices 
curled over backward; lip with a broad downwardly directed 
median lobe, lateral lobes hardly developed, basal part bulbous; 
column with anthers about 28 mm. long, very stout, the rounded 
apex very faintly suffused with purplish; the four pollinia bright 
orange, on a clear white stalk; callus of lip very thick, about 7.5 
mm. broad, suboval, pale orange tinted. The flowers are not 
s'icky or aromatic. 

In addition to the above and the true L. Skinneri Lindley, we 
have Lycaste cruenta Lindley, belonging certainly to a distinct 
section of the genus. . The sepals are very sticky on the outer 
side, and the flowers have a strong aromatic odor. It is also 
peculiar in that one of each pair of pollinia is about a third 
smaller than the other. The following description of the flower 
is from life: 

LYCASTE CRUENTA Lindley 

Scapes about 14 cm. long; bracts 4-5, dark red brown, sheath- 
ing, loose, pointed, uppermost about 22 mm. long; flowers erect, 
about 40 mm. long, brilliant orange, with the broad sepals pale 
yellow-green; sepals about 50 mm. long and 24 broad, oblong, 
rather obtusely pointed, bearded at base within; petals shorter 
than sepals, more ovate, with a larger apical angle, lightly speck- 
led with crimson at base; lip abundantly spotted with crimson 


12 


within, but the extended, downwardly curved median lobe not 
speckled, its apical margin slightly irregularly crenulate but not 
fimbriate; column about 16 mm. long and 7.5 broad, flattened, 
but thick, dark crimson at base, the contiguous part of the lip 
also crimson, and the at base of the lip on the outer side is a 
transversely elongate crimson patch. 


— 


SHORTER NOTES 


PLANTS IN FLOWER IN THE AUTUMN OF 1918 ON LonG ISLAND, 
N. Y.—Weather Bureau records confirm the observations of 
everyone that October was the warmest ever known in this vi- 
cinity. Certain days of almost summer heat were warmer than 
any October day for as far back as the records go. It is probably 
due to these unseasonably warm October days that the following 
list of plants in fresh flower on October 28-30, and November 1-2, 
can be recorded. 

PLANTS IN FRESH BLOOM AT GARDEN City, L. I., on OCTOBER 


28-30, 1918: 
Trifolium pratense Solidago juncea 
fe repens Brassica sp. 
oN arvense Daucus carota 
Linaria Linaria Melilotus alba 
Taraxacum Taraxacum Achillea millefolium 
Aster paniculatus Chrysanthemum Leucanthemum 
“ dumosus Neopieris mariana (Nov. 4) 
‘““ ericoides Baptisia tinctoria (Nov. 4) 


During a walk from Pine Lawn to Lake Ronkonkoma on 
November 1-2, with Mr. Norman Taylor, the following were 
also found in fresh bloom: 


Aster ericoides Houstonia longifolia 
‘undulatus Cichorium Intybus 
‘*  divaricatus . Taraxacum Taraxacum 
' s scordifolus | Prunella vulgaris 
‘“ novae-angliae Daucus carota 
‘““  Jateriflorus Achillea millefolium 
~< patens Chrysopsis mariana 
‘““ -vimineus Linaria Linaria 


Tradescanti Oenothera biennis 


Solidago juncea 
nemoralis 
bicolor 
puberula 
rugosa 
caesia 
Ionactis linariifolius 
Centaurea Jacea 
Trifolium repens 


ac 


pratense 


agrarium 
sf arvense 
Rudbeckia hirta 
Viola pedata 


Verbascum Thapsus 


13 


Oenothera muricata 
Melilotus alba 
Nabalus sp. 
Rubus sp. 
Erigeron ramosus 
‘ canadensis 
Gnaphalium obtusifolium 
Plantago lanceolata 
- aristata 
Chrysanthemum Leucanthemum 
Brassica sp. 
Lepidium 
Hieracium scabrum 
Polygonella articulata 
Dianthus Armeria 


Persicaria pennsylvanica Eriocaulon septangulare 


WILLIAM C. FERGUSON 
GARDEN CITY. 


CONCERNING Duplicate TypEs.—In the extensive array of 
names compounded with ‘‘type,’’ all of which agree in present- 
ing some idea derived from or modifying the meaning of that 
word, it seems strange that the conception which we taxonomists 
most often have occasion to designate appears not to have re- 
ceived any mononomial term. I allude to that which some of us 
have erred in calling ‘‘co-type,’’ and to which others, more con- 
sistent, have applied the phrase ‘‘duplicate type’”’ or ‘‘duplicate 
of type.”’ 

In 1905, Dr. A. S. Hitchcock indicated the distinction between 
duplicate type and co-type. In Science 21: 832, he defines a 
duplicate type as a specimen ‘‘of the same series or set as the 
type as indicated by the number or other data,” and a co-type 
as a specimen “‘cited with the original description in addition 
to the type specimen.’”’ In actual practice, in explaining our 
application of names, we continually need a short expression for 
the former—something as simple and easily remembered as the 
really less important word co-type. To meet this need I sug- 
gest the term isotype. 


14 


The word isotype, compounded from the Greek, means “‘equiv- 
alent to the type.’ To offset the objection that a duplicate is 
not necessarily equivalent to the type, indeed too often is quite 
different, is the fact that it always should be the same and so for 
the purpose of comparison should be its equal in value. Per- 
haps the best raison d'etre which can be urged for a word is its 
suggestion of an ideal; such a term should emphasize the import- 
ance of all duplicates being thoroughly like the type.—FRANCIS 
W. PENNELL. 


REVIEWS 
Boerker’s Our National Forests* 

A short popular account of the work of the United States For- 
est Service on the national forests, by the arboriculturist of the 
Department of Parks, New York City. The introduction (pp. 
xiii-xlvii) is followed by four chapters on the creation and or- 
ganization, the administration, and the protection of the national 
forests, and the sale and rental of national forest resources. An 
Appendix of six pages contains a tabular statement of land areas 
within the national forest boundaries. 

The book, well illustrated, brings together in small compass, 
reliable information on a subject about which every citizen should 
be intelligent, but which has hitherto been largely inaccessible 
on account of being widely scattered in Government bulletins 
and reports. Some of the information will be a revelation to 
perhaps the majority of readers. For example, we learn (p. 72) 
that the Forest Service has, since 1911, collected over 175,000 
pounds of tree seeds for planting, and that 21 tree nurseries, in 
1916, had in them over 37 million young trees to be planted in 
reforestation work. The average layman, who possesses chiefly 
misinformation concerning the relation of forests to climate, will 
profit by reading the author’s paragraphs on that subject (pp. 
89-92). Those who are still skeptical (and there are many such) 
as to the practical value of preventive and remedial measures 
for tree diseases and pests will be enlightened to learn, merely 
as an illustrative example, that an expenditure of only $3,000 


* Our National Forests. By Richard H. Donai Boerker. New York. The 
Macmillan Co. 1018. $2.50. 


15 


for insect control on about 900 acres in the Klamath National 
Forest, resulted in a saving of timber to the value of over 
$600,000 (p. 96). 

Friends of conservation will be interested to learn (p. 114) 
that a single issue of a New York Sunday paper consumes the 
trees on about 15 acres of forest. Apropos of this, one may per- 
haps be pardoned for questioning the wisdom, or the advantage 
from any point of view, of using eleven pages (pp. lix—lxix) to 
repeat in full the legends of the 80 illustrations. The analytical 
table of contents hardly makes up for the absence of an index. 
Incidentally it might be remarked that the fringed edges (tech- 
nical term unknown to the reviewer—chewed would be appro- 
priate) make it necessary to use the carpet sweeper and whisk 
broom after one has spent an hour with the book. 

But the few features that may be noted adversely are minor 
matters in comparison with the general excellence of the book. 
It gives a terse and readable survey of the history and activities 
of the Forest Service, and makes clear the need and value of 
this work. It will be invaluable as a reference book in all col- 
leges and universities, and in public and private libraries. Both 
the author and the cause of forestry and conservation are to be 


congratulated. 
C. STUART GAGER. 


Harwood’s New Creations in Plant Life* 


The revised and enlarged reprint of the first edition of W. S. 
Harwood’s ‘‘ New Creations in Plant Life’’ reads like a Florida 
land investment prospectus or a modern version of ‘‘ The Arabian 
Nights.” 

Mr. Harwood tells the story of Luther Burbank and his work 
with all the enthusiasm, all the veracity, and all the inspiration 
one expects from one whose years have been devoted to journal- 
istic effort. In Chapter I is recounted the struggles and tribu- 
lations of Burbank, the man, toward accomplishing his life’s 
ideal. ‘‘Now and again,’ Mr. Harwood writes, ‘‘arose some 
pseudo-scientific man who, professing unlimited friendship, 


* Harwood, W.S. New Creations in Plant Life. 2d ed., Revised and Enlarged. 
Pp. xviii + 430. Illustrated. The Macmillan Co., N. Y. 1918. Price $2.00. 


16 


sought for means to filch the rapidly increasing reputation. 
Others visited him with the covert purpose of exposing him as 
a charlatan after inspecting his methods, but, confounded by 
what they saw, went down the little hedge-bordered walk that 
leads to his quiet home shamed into silence.” 

Chapter II details the methods of work of this horticultural 
wizard. On pages 40-43, a list of some of the miracle-like ac- 
complishments are set forth. Among these are “‘The improved 
thornless and spiculeless edible cactus, food for man and beast, to 
be the reclamation of the deserts of the world’’; the union of the 
plum and the apricot, said to be an impossible accomplishment; 
a plum with a Bartlett pear flavor; a tree which grows more 
rapidly than any other tree ever known in the temperate zones 
of the world; a dahlia with the scent of magnolias, a calla lily 
with a Parma violet’s fragrance, a chestnut tree that bears in 
eighteen months from seed, an amaryllis with flowers nearly a 
foot in diameter, a calla with flowers 10-12 inches across, a rare 
fruit called the pomato, ‘“‘which grows upon the top of a potato,” 
and soon. This genius, according to Mr. Harwood, so remark- 
ably possessed with horticultural intuition, has bred the pits out 
from the plum, the bitter tannin from the English walnut, given 
a trailing-arbutus perfume to the verbena, created new species 
long thought impossible, taken the horrid thorns off from black- 
berries, and make them beautifully white in fruit. All these 
have been accomplished and the “‘half has not yet been told.” 

On page 51 is computed the gross financial returns for 160 
acres of average farm land for 12 years if planted to one of Bur- 
bank’s hybrid walnut creations. The sum is $485,000, very 
nearly half a million. The expenses to be deducted from this 
in the form of care, taxes, etc., are said to be small. On 
page 68, a paragraph is devoted to Mr. Burbank’s work on the 
chestnut. Ordinarily, we are told, the chestnut trees raised from 
seed are from 10 to 25 years old before they bear nuts. Now 
this was altogether too slow for these modern days, so Mr. Bur- 
bank produced a tree that bears nuts when seven months to a 
year anda half old. The readers of this review, possessing desert 
properties not accessible to irrigation will be interested in state- 


17 


ments of an annual yield per acre of 20 tons of spineless cactus 
which can be utilized for cattle food. In tropical climates, where 
the land can be irrigated lightly once or twice, an annual yield 
of 150-180 tons per acre may be expected. As contrasted with 
100 acres alfalfa under the best conditions, the yield of Burbank 
cactus under equally favorable conditions would be 30 to 40 
times, we are told on pp. 390-391. And the best of it all, ac- 
cording to our author, is ‘‘that once established, the new cactus 
may remain for years uncultivated and undisturbed, constantly 
growing on and adding to its vast store.” 

To the flower lover, the account of Burbank’s work with pop- 
pies will surely be of absorbing interest. On page 79, a Burbank 
poppy is described with flowers, a dozen of which placed one 
upon another, would effectually conceal a man—seven of these 
magnificent blossoms placed end to end in a row are as high as 
a tall man. 

The volume is well and quite copiously illustrated and no one 
interested in flowers, fruits, and plant life in general can help 
being fascinated and very much impressed with this account of 
the wonders an untrained and comparatively uneducated man 
has produced in the plant world through using his intuition. 

ORLAND E. WHITE. 


PROCEEDINGS OF THE CLUB 
OCTOBER 30, 1918 


The meeting was held in the Morphological Laboratory of the 
- New York Botanical Garden, at 3:30 P.M. There were thirty 
persons present. Vice-president Barnhart occupied the chair. 

The minutes of October 8 were read and approved. 

The nomination and election of M. Nishimura, Columbia Uni- 
versity, N. Y. City, and Dr. Thos. Owen, Dept. Archives and 
History, Montgomery, Alabama, followed. 

A communication from Prof. J. E. Kirkwood relating to the 
publication of a paper as one of the Memoirs of the Club was 
read and referred to the Board of Editors for a report. 

The scientific program for this meeting consisted of an “ Ex- 


18 


hibition of a Collection of Flowering Plants and Mosses from 
North Star Bay’’ made by Dr. E. O. Hovey on the Macmillan 
Expedition. Dr. Hovey then gave an illustrated lecture on “ De- 
scription of the Habitats of the Plants Forming this Collection.” 

“The collection of plants made by Dr. Hovey at North Star 
Bay, 78 degrees 30 minutes N. latitude, was exhibited by Mrs. 
N.L. Britton. It included a few flowering plants, Arnica alpina, 
Casstope tetragona, Dryas integrifolia, Papaver radicatum, Ranun- 
culus nivalis and Saxifraga oppositifolia, as well as three dwarf 
willows, Salix herbacea, S. groenlandica, named by Dr. Rydberg, 
and a larger species of willow still undetermined. Of the flower- 
less plants, 25 are mosses, 8 are hepatics, five are lichens, and two 
are fungi, one a Mycosphaerella, parasitic on the leaves of one of 
the willows and the other a mould (Mucor sp. ?), which seems to 
be abundant at North Star Bay. The collections were studied 
by Dr. Evans, Dr. Andrews, Dr. Seaver, Miss Coker, Mr. Wil- 
liams and Mrs. Britton. After examining the specimens the 
Club adjourned to the lecture-room, where Dr. Hovey showed 
some beautiful views of North Star Bay and its flora, including 
some excellent photographs of birds and a few of the Esquimaux 
and their dogs.” 

Adjournment followed. 

B. O. DODGE, 
Secretary. 
NOVEMBER 12, 1918 

The first meeting in the month was held at the American 
Museum of Natural History. There were twenty-one persons 
present. Prof. R. A. Harper.was elected chairman and called © 
the meeting to order at 8:26 P.M. The usual order of business 
was dispensed with. 

Dr. Geo. E. Nichols delivered the lecture of the evening, the 
subject being, ‘‘The Sphagnum Moss and its Use in Surgical 


’ 


Dressings.’’ The speaker first described and illustrated several 
of the more common species of Sphagnum to be found in North 
America, calling attention to the differences in size, color and gen- 
eral habit existing between species. The marked variation in 
individuals of the same species was also noted as being due to 


19 


climatic or environmental influences. The morphological char- 
acters of the stems and leaves were described and the particular 
features by virtue of which the dried moss is able to absorb such 
large quantities of water were pointed out. It was shown that 
dried Sphagnum is capable of absorbing as much or more per dry 
weight as the ordinary absorbent cotton used in making dressings. 

The cells of the leaves are of two sorts. The smaller or nar- 
rower cells making a network, are green, while lying between 
the green cells we find much larger, empty cells whose walls are 
provided with large pores through which water may be absorbed 
from the outside. These cells are also characterized by thick- 
ened bands which serve to strengthen the system. 

Numerous specimens of Sphagnum were exhibited. The meth- 
ods by which the moss is harvested, dried, sorted and made into 
surgical dressings were described. 

A number of the various kinds of dressings made with Sphag- 
num or with cotton were shown. The lecture was illustrated 
with lantern slides. It has been published in part in the Journal 
of the New York Botanical Garden. 

Adjournment followed. 

B. O. DopGE, 
Secretary. 


NEWS ITEMS 


At the annual meeting of the Club held on January 14 the fol- 
lowing officers were elected: President, H. M. Richards; Vice 
Presidents, J. H. Barnhart and C. Stuart Gager; Secretary and 
Treasurer, B. O. Dodge; Editor, A. W. Evans; Associate Editors, 
Jean Broadhurst, J. Arthur Harris, M. A. Howe, M. Levine, G. 
E. Nichols, A. B. Stout, and Norman Taylor. Dr. M. A. Howe 
was elected as the delegate of the club to the Council of the 
New York Academy of Sciences. 


Prefessors Edward W. Berry and J. T. Singewald, Jr., of the 
Johns Hopkins University are planning to leave in April for a 
six months trip of geological and paleontological exploration in 
the Andes. The region that they will cover extends from Peru 
to southern Chile. 


20 


Dr. E. W. Olive, of the Brooklyn Botanic Garden, spent some 
time during the past summer assisting government and state 
agents in locating plant diseases and instructing farmers how to 
combat them. An account of his experiences in part of New 
York and Virginia was given ina public lecture at the New York 
Botanical Garden on October 26, and was accompanied by lantern 
slides illustrating some of the most important and recently intro- 
duced diseases. Among these were the nematode disease of 
wheat found in Virginia and the potato wart disease discovered 
in Pennsylvania. 


We learn from Science that Professor F. C. Newcombe of the 
University of Michigan “‘has been granted leave of absence for 
the second half year on the condition that he supply a substitute 
at his own cost.’’ Professor Newcombe has been at the Uni- 
versity since 1890. 


Dr. L. T. Knight has been appointed plant physiologist in 
the division of plant pathology at the Minnesota experiment 
station. 


Barrington Moore, formerly Associate Curator of Woods and 
Forestry at the American Museum of Natural History, and for 
sixteen months with the American Expeditionary Force in France, 
has received his discharge from military duty. Major Moore 
assisted Lt. Col. H. S. Graves, chief of the United States Forest 
Service, in organizing the forestsy troops which produced lumber 
for the A. E. F. Major Moore later had charge of all purchases 
of wood in France and other European countries for the Ameri- 
can Army. At the Baltimore meetings he was elected president 
of the Ecological Society of America. 


Dr. F. W. Pennell, of the New York Botanical Garden, is 
spending some time at the United States National Herbarium 
studying the collections made in South America by Dr. J. N. 
Rose. 


The conservatories of the Brooklyn Botanic Garden, which, 
owing to shortage of coal and consequent crowding of the col- 
lections have been closed for over a year, have been reopened. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of ToRREYA in which their papers appear, will kindly notify the 
editor when returning proof. 

Reprints should be ordered, when galley proof is returned to the editor. The 

“New Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
following rates: 


2pp 4pp 8pp 12pp 16pp Z0pp 
25 copies $ .79 $1.14 $1.78 $2.32 $2.87 $3.28 
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200 copies 2.15 3.24 3.92 5.25 6.52 6.92 


Covers: 25 for $1.00, additional covers 114 cents each. 
Plates for reprints, 50 cents each per 100. 


Committees for 1919, 


Finance Committee Program Committee 
R.A. HARPER, Chairman. Mrs. E. G. Britton, Chairman. 
J. H. BARNHART, Pror. JEAN BROADHURST 
Miss C. C. HAYNES B. O. DopGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F. J. SEAVER 
J. H. BARNHART, Chairman. Membership Committee 
R. A. HARPER J. K. SMALL, Chairman. 
N. L. Britton T. E. Hazen 
A. W. EVANS E. W. OLIVE 
M. A. Howe Local Flora Committee 
Hi. H. Rusgy ; N. L. Britton, Chairman. 
Field Committee Phanerogams: Cryptogams: 
F.W. PENNELL, Chairman. E. P: BICKNELL Mrs. E.G. BRITTON 
Mrs. L. M. KEELER N. L. BritTon T. E. HAzEN 
MICHAEL LEVINE C. C. Curtis M. A. Howe 
GEORGE T. HASTINGS K. K. MACKENzIE MICHAEL LEVINE 
PERCY WILSON NORMAN TAYLOR W. A. MuRRILL 


F. J. SEAVER 
Chairmen of Special Committees on Local Flora 
_ Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M. 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M. Richards, F. 
_ Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 
Cortinarius: R: A. Harper ‘Zygomycetes: A. F. Blakeslee 
Polyporeae: M. Levine’ _ Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
’ Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurst 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


OTHER PUBLICATIONS 


OF THE 


TORREY BOTANICAL CLUB 


(1) BULLETIN _ 

A monthly journal devoted to general botany, established 
1870. Vol. 45 published in 1918, contained 519 pages of text 
and 15 full-page plates. Price $4.00 per annum. For Europe, 
18 shillings. Dulau & Co., 47 Soho Square, London, are, 
agents for England. 

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Vol. 19 February, I919 No. 2 


TORREYA > 


A Monruiy Journat or Boranicat Notes anp News 
EDITED FOR 


SHE TORREY BOTANICAL CLUB 


8Y 


NORMAN TAYLOR 


fOHN TORREY, 1796-1873. 
CONTENTS 
Botanical Study of Skunk Cabbage: KATHERINE As WILLIAMS..+- 0.) -sseceeers eevee ese at 
Some Remarks upon Limosella; F. W. PENNELL .-.-- 1.16 ceeneeey cece cene cree ct eee eee e ees 30 
in tie: Wake of the Hnemy 15.5% Pe 4 hcoakh. 3 ses dasa tas Uadioens nose ps cabs vine oe Pade ee 32 
Proceedings of the Club ....... WE TR GS CMR IAL Sanaa MAL RMSE, Pa EAR Aa eb Rae 33 
TMM IM GOSIAR DICER Ci 5.5 ca.) Soont bate oleayaek eens cone he faaeed Mice veudgee SMe ae th wpSeh hen syrs 34 
BWIA ECE TINGS vcs. 5s aap aes nchh “Soaliu gas Daceensse ped eure tepeccus cape wy Byte Del ORR S as 5 rae 36 


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Vol. 19 No. 2 
February, IgIg 


A BOTANICAL STUDY OF SKUNK CABBAGE, 
SYMPLOCARPUS FOETIDUS 


By KATHERINE A. WILLIAMS 


The skunk cabbage is a plant of unusual interest and wide 
distribution, and although its general growth and morphology 
are pretty well understood, little has been done in an exact study 
of the plant. A recent study of its western congener, Lysichiton 
Kamtschatcensis, has emphasized the importance of a detailed 
investigation of the eastern swamp plant. This study was begun 
early in the spring of the present year (1918) witha view tomakiag 
known some of the features of the plant which have not been 
emphasized in previous descriptions of it. In the prosecution of 
this research, I have been assisted by the helpful suggestions of 
Prof. John W. Harshberger, under whose direction the work has 
been prosecuted throughout. 


PHYTOPHENOLOGY AND DISTRIBUTION 


Phytophenology—The skunk cabbage is one of our earliest 
forest plants, for records show it blooming even in the late fall, 
or early winter. According to the records made by Dr. Marion 
Mackenzie and presented before the Botanical Society of Penn- 
sylvania, flowering specimens have been found as early as Novem- 
ber twenty-first. Also when the year is backward for any reason, 
the flowers have been even as late as March before opening. 
The average date of first blooming seems to be about the middle 
of January, as seen from the following table. This year the 
flowering was somewhat later than usual. 


(No. 1, Vol. 19 of TorREyA, comprising pp. I-20, was issued 21 February 1919] 


2] 


LDR, 
NEW y 
SOTAN; 
GARD: 


bo 
i) 


Date of Opening of 


Year First Flower 
TSO OMe ae mere ne Sones ees eee March 8 
TOOOR est 27: SE SO see Ces ee February 22 
TOOT Wey este te ere ai cee te oe ear ee February 18 
THOVO PD Ga oped gah a So cor Saye eee ee January 27 
TO) GAs caine chces PRRs pata ccl eee Silos January 15 
LOOM Sete ea eee Para ne Wares ehedn coo January 23 
TO OS ee et eee te ee et January 18 
LOO OMe a eee yore ore A cd January 5 
MOOG eo aah a ear tee January 10 
TOO Se eee ee eee os BiseInS January I 
TGYOC Soe S Sets orca eee ea November 21 (1908) 
TOUS es ee ee toy oaearst sk Heese sere March 9 


Daily more and more flowers open until about the latter part 
of February and early March when they are at their height. 
Then the greatest numbers may be found open. Of course the 
date varies slightly owing to the general weather conditions. 

Distribution.—In general the plants are found in the eastern 
coastal states, although a closely allied species is found through- 
out the west and is there spoken of as the western skunk cabbage, 
or Lysichiton Kamtschatcensis. It is common around Vancouver. 
In general, though, Symplocarpus is distributed along our eastern 
states, ranging from Nova Scotia down to Virginia and is also 
reported by the Gray Herbarium of Harvard University, as 
having been found in Amur and Japan. 

The following table gives in general its distribution. 


Number of Herbariums 


States Reporting 
(CHiTEGIIS Sos oo nee ee re Cocks, < ola cs 2 
IMDS seca otk Ie Chae eee wee EREe Carte eater One ois So. Bio.s c 3 
INJSG7 [Biya oh tae 2 5 Core Se Pea ere ete Hors boca Z 2 
WSR 55 bit ain co On Aone oe ene eneeia croc cxdehebo ar I 
IMME REACTS S HICS 4 SES a eee ce nes aid 4) Glo ExS - 4 
[pelsveete: IE Wael 5 Son ead eee Re ace beter cco © om pekoor 2 
(CENTOS MONE 6 In FAO CERO ROIS a oe re © 4 
ibys Wj Eyavel 045 Se sig Baas oe OED porto oud. ° 2 
ID feXy Nord oe Aa eae eee PER aS ele S 3 
inifesiie TGEESY: oo 0s St erect eee Pe eeemen ater chrcec co C5. 3 
Pains wlvalaeseitt sect oh. clase os date SS ee 2 
Districtiot Columbias.:..--....- Sgt a cautacie Sin ee I 
WistadbeiiGl say An Svs OU peo Gore Ree aC eeIEeITSaee Ter I 


WIGGIMIAS bist tie oo een clat eos hy - Bed ky Rh hoe I 


23 


Number of Herbariums 


States Reporting 
SROTIMOAREE Ome he cena ale is ig die ad ak ty Bike Reel Gul a I 
Lay rs! Lai, Ce SE Site RS SES ie nee or Renae I 
Rerelicttict naar Sa eon eee ears ea late eveiatatw ll} a wis eeRia’ © a%e I 
Ie RE ee Riot Re Nee ates Be coy date 2 
RUST CUTS ATE hed Here tie cna sete i Days wo oe ior wna a one ea 2 
PU ER OETISITES ig Mee OPES twin eS eee ews hoe pees Pite ¥ 3 
Rtn erotae a, Mele ce tote orale cic ocx wets Boi etepeeieer I 
INTER A OCOLIACE Some retest een ere oe tines et eon ge area 2 
ONE BEC. sclee ote Ae oe eka the Oy et alle einer se eee I 
PU ise bapa Ae see, See oak pea eden yo Me Cae, Sr Sa I 
| EOE a Regen Bee 2S y5 ie ci Pease he Puen MIR Ay ey I 


Symplocarpus, like some other members of the Arum family, 
grows best with a great deal of moisture. And it isin the swamps, 
marshes and bogs or stream beds, that these sturdy plants are 
usually found. 


GENERAL STUDY 


The skunk cabbage, or Symplocarpus foetidus, is really our 
earliest spring flower. 

Odor of Plant.—Knuth in his classification of flower odors 
describes it as nauseous and of mephitic, or viverrine, type. In 
another case, I found it described as an odor that combines 
the skunk, putrid meatand garlic. Still another writer describes 
it as being a combination of a mustard plaster and raw onions. 
To me the odor is not especially repulsive. It suggests that of 
fresh cabbage with a slight suggestion of mustard. To some, 
however, the smell is quite repulsive. 

The odor varies in intensity and quality quite widely. Those 
plants in which the stamens are ripe seem to have the stronger 
odor. This is probably due to the greater maturity of the plant 
at this stage of flowering and it has the added significance of 
attracting a greater number of insect visitors. 

Origin of name.—The origin of its common name is not diffi- 
cult to ascertain, for on crushing the plant immediately an odor 
arises something like that of the cabbage with yet a suggestion 
of the mephitic skunk. 

The generic name of the plant, Symplocarpus was given to it 
by Richard Anthony Salisbury, and is derived from two Greek 


24 


words ovurdoxy, Meaning connection and xapzés, fruit. This is 
quite appropriate, since the ovaries unite to form a compound 
fruit. Linnaeus gave us its specific name of foetidus. Many 
scientists use the term Spathyema, as given by Rafinesque. A 
point interesting in regard to its name is that the early Swedish 
settlers around Philadelphia called it bear-weed, because the 
bears relished the early green food and feasted on its leaves, 
which are quite large and conspicuous, like coarse cabbage leaves. 

Order and family.—We have heard so much about its disagree- 
able odor that we hardly realize that it belongs to the same family 
as our Calla lily, for it is a member of the family Araceae. Ac- 
cording to Gray, “they are plants with acrid or pungent juices, 
simple or compound often veiny leaves and flowers crowded on a 
spadix which is normally surrounded with a spathe.”’ Other 
closely allied plants, which we find around here, are the golden 
club, so common in Jersey ponds and the familiar jack-in-the- 
pulpit. Neither of these, however, possesses the pungent odor, 
but the Jack, or Indian turnip, is like Symplocarpus in that it has 
many crystals found in the root, which give it a biting clawing 
taste. 

EARLY GROWTH 


Flower, spathe—The first signs of the plant are the sessile 
hood-shaped spathes which come up though the ground early 
or late in the winter, even when the ground is hard with 
ice at a foot’s depth. The flowers are included in a thick 
leathery spathe. This in general is like a hood, or even shell- 
shaped. It is sessile and grows close to the ground. In most 
instances, it has the same general form, although there is a wide 
variation in contour, size and coloring. Some of these leaf-like 
spathes are deeply curved, others stand more erect. Some are 
found which are double. In this case there seems to be a 
spathe inside a spathe, the open part of the outer spathe 
coming against the rounded back of the inner spathe. Also in 
such cases the innermost spathe seems to have a longer, more 
leaf-like tip which projects backward and out beyond the outer 
spathe tip. One plant was found this spring (1918) at South 
Springfield, Pa., with four double spathes. 


b 
or 


The greatest variation is seen in the coloring. Usually this 
ranges froma deep purplish-red, almost black, to a pale yellowish 
green. Spathes may be found showing the different colors and a 
complete gradation shown from the light to the dark. The 
lighter spathes are rarely ever pure pale green, but more fre- 
quently are mottled with the deeper purple. In some instances 
the inner side of the spathe is deeper colored than the outer. 
The mottling is such that it closely resembles the flickering 
lights and shades often seen on the undergrowth, as the sun 
filters through the leaves of the trees overhead.’ This frequently 
makes it hard to find them on the forest floor. Reed suggests 
that this variation is due to age, the younger blooms being those 
lighter in color, while those which are darker are the older ones. 
This did not seem to hold true as regards the plants observed 
by me. Out of about fifty examined for this peculiarity, 
withering and decay was not limited to the dark ones alone, 
but was seen in spathes of all intermediate shades of coloring. 
Again it was suggested that the water content of the soil might 
lead to this variation. Some time spent on this study did 
not seem to prove this to hold true, as two spathes from the same 
plant, side by side, showed one a deep reddish purple and the 
other quite pale. VAs 

The flowers themselves are crowded together on a short stalk 
or spadix. They are really quite inconspicuous. It is the spathe 
that is the attractive portion, as far as coloring and conspicuous- 
ness are concerned. The flowers themselves are closely crowded 
on the spadix, so closely crowded that they hardly appear as 
individual flowers. Thestamensand pistil only are conspicuous. 
The flower cluster varies in size and in the number of flowers 
produced. Showing this variation we have the following table. 


Size relatively Size in inches No. of flowers 
SOMA heg eta: 5 ese cho alee see at 5/8” 38 
Wein. Wie, aradacheiet ee 7(8” ae 
WATEC 2 lai ho dinc.e ost cyan ae 7/8” 69 
WErV lab PCa ies). a.5 aceb ener 13/16” 61 


The-flowers as shown by the figures are closely crowded together. 
In this case, the spadix of medium size had the greatest number 
of flowers. And the largest spadix had only 61 flowers. 


26 


It is due mostly to this crowding that the flowers have departed 
somewhat from the usual monocotyledonous habit of having 
three, or its multiple, in their floral parts. In general the flowers 
showed four perianth parts. These were almost cuboidal in 
shape, when pressed close together, and they overlapped each 
other, making a box-like arrangement. The four stamens have 
long flat, broad filaments and straw-colored anthers, which pro- 
trude beyond the perianth segments. The stamens are arranged 
opposite the perianth parts. The anthers are two-celled, opening 
lengthwise and are extrorse and rather free in their movement. 
The flowers are protandrous, the anthers developing earlier 
than the pistil. The pistil is unusual in its general structural 
form. The stigma is three-lobed, the style is cuboidal and the 
ovary is one-celled. : 

In a cluster of about 73, some flowers showed a few variations. 
These were either near the lip or the base where less crowded. 
It seemed an attempt to revert to the usual number of parts in 
the lilaceous monocotyledones. Four specimens were found 
having six stamens and six perianth parts. Another flower showed 
five stamens and five perianth parts. And still another specimen 
was found having four stamens, but with six perianth segments. 

The color of the flowers, according to one author, resembling 
decayed flesh, combined with the odor which is doubly suggestive, 
attract carrion-loving flies of the family Diptera, which are useful 
in the pollination of the closely crowded, otherwise inconspicuous 
blossoms. 

Insect visitors —From a recent article in American Forestry 
by R. W. Shufeldt, I find that a variety of bee introduced into 
this country from Europe is one of the earliest visitors, since they 
must have food early in the spring: The article further states 
that the honey bee, if able at all to enter, finds the exit too narrow 
and slippery and the bee perishes miserably. Another curious 
fact he has noted also is the frequent presence of spiders’ webs 
at the entrance to the spathes. This fact was also noted by me. 
It is a case where the flower odor attracts the flies, and they in 
turn are entangled in the spider’s web and so furnish food for 
the spider. 


bo 
~] 


Shortly after pollination the spathe begins to decay and 
wither and the spadix to swell. It becomes soft and spongy and 
the individual fruits are covered with a papery skin-like sheath 
under which the seeds develop. These when mature are hard, 
round, dark brown and somewhat irregular in shape. In fact, 
they look a little like pebbles or stones. When fully ripe they 
break the sheath, fall to the ground and germinate the following 
spring, giving rise to new plants. A parent plant may be found 
having many seedlings coming up close around it. 

In germination a small pointed, closely coiled shoot first 
appears above the ground. This is carefully wrapped in the 
thin papery sheathing leaves. When about a week old this 
shoot is about an inch in length. A few slender fibrous roots, 
rather long and thin grow downward into the ground. As yet 
there are not many roots to nourish the plant; these few primary 
roots have thread-like secondary roots. 

By the second week, the seedling has grown much larger and 
the tip of the shoot has become freed from its papery sheath. 
This however grows along with the young plant. Also by this 
time a rootstock begins to develop. There are also many more 
roots, long, thin and tapering. 

At the third week, the shoot has broken through both 
sheathing leaves and is quite large.- At this time the seedling is 
about four inches tall. It has severed its connection with the 
remains of the seed by this time. From now on development 
consists of growing larger and larger rapidly. This plant how- 
ever does not bloom the first year. Nor am I able to tell by 
actual observation, since my study has covered only a period of 
five months, how many years elapse before the plant has grown 
old enough to produce its first inflorescence. Probably the 
flowers are produced the fourth year. 

That the plants develop more rapidly and better in warm, 
light places is seen by the table given by Dr. Mackenzie in her 
report before the Botanical Society in r911. Also in some speci- 
mens which I brought in from the wood, the uncurled spire of 
leaves, just barely sticking above the soil, soon came into full 
leafage, in the warmth of the greenhouse. The plants had been 


28 


set aside in a bucket of water, as of little further use. In less 
than a week after bringing them in about six leaves were fully 
uncurled and widely spread. 

The leafage of the plant is quite interesting. Soon ane the 
blossoms appear, a small whitish shoot is seen forcing its way 
above ground. On going one can see that it consists of two 
almost whitish sheathing leaves. These show the monocotyle- 
donous character in having parallel veining. Closely rolled inside 
of these are the true leaves. They form a light hard-coiled 
center. The tips, when they have broken through the enveloping 
sheath-like leaves, are frequently colored purplish like the 
spathe of the plant. Such coloring may show on the outside 
of the tip of the first and even the second leaves. These inner, 
or true, leaves seem to break away from the monocotyledonous 
and tend toward the netted veining of dicotyledonous plants. 
The first three leaves unfolding show a gradual transition toward. 
the netted veining of the later leaves. In all the cases the veining 
is palmately netted. Also in specimens planted under dry con- 
ditions, in a pot in a frame, and those under moist conditions, 
the plants grown under dry conditions tended to show the netted 
veining earlier than those of the moist environment. 

The leaves when fully developed are quite large, being some- 
times over a foot in length and at least eight or nine inches broad. 
They have an entire margin and are of a bright green color, rather 
shiny in appearance. They grow rankly in a rosette form, in the 
damp stream beds. Their great size makes them very con- 

spicuous. 

In a microscopical study the leaves show raked large air 
chambers and loosely packed cellular structures. Throughout 
the leaf are various rhaphides occurring in the large bundle 
masses. There. are also several other types of crystals, a few 
cuboidal in shape, and even some spherical in shape may be 
found scattered loosely here and there—sphaerocrystals. 

Juice—The juice of the skunk cabbage is very bitter and 
acrid. This when tasted in the fresh plant had a peculiar garlic- 
like taste and seemed biting. By biting I mean the prickly 
sensation very much like that experienced on eating the root of 


PLATE II 


29 


the jack-in-the-pulpit. When the plant was cooked, the water 
was the color of weak tea and the plant itself lost most of its 
flavor and the property which gave it the biting character. 

Roots.—The plant is a very difficult one to collect in its 
entirety, owing to its immense rootage. One must dig over a 
foot down into the soil before there is even the slightest sign of 
the roots giving way. There is a large central root-stock almost 
the size of a potato and from this great numbers of roots arise 
and grow downward for almost two feet in length. They are 
very long, rather straight and unbranched excepting for a few 
almost thread-like offshoots. | 

All the older roots are peculiar in having ring-like markings or 
wrinkles on them. These are especially seen near the upper or 
older end of the root. They are contractile roots and are peculiar 
to a few plants. Their general purpose is to pull the plant back 
into the ground as it grows up every year. By a process of 
contraction the roots wrinkle up and draw the plant down into 
the soil. The roots are permanently wrinkled after this con- 
traction. 

The root structure shows large loose cells and a single, radial 
central stele. The cells around the outer cortex, near the epi- 
dermis are particularly loose. This is due to the contraction 
of the epidermis. 


DEPARTMENT OF BOTANY, 
UNIVERSITY OF PENNSYLVANIA 


EXPLANATION OF PLATES 


Fig. 1. Outside of Spathe of Skunk Cabbage. 

Fig. 2. Double Spathe. : 

Fig. 3. Dissection of Spathe to show Spadix with Flowers. Spadix with extra 
long Peduncle. 

Fig. 4. Single Flower of Skunk Cabbage. 

Fig. 5. Flower with depression of two outer Perianth Segments. 

Fig. 6. Flower laid open showing four Stamens and Pistil. 

Fig. 7. Floral Diagram. 

Figs. 8,9, 10,14. Early Stages in the Germination of the Seeds of the Skunk 
Cabbage. 

Fig. 11. Closely rolled Leaves with Netted Veining. 

Fig. 12. One of the first and outermost Leaves with Parallel Veining. 

Fig. 13. A contractile Root. 


30 


SOME REMARKS UPON LIMOSELLA 


By FRANCIS W. PENNELL 


Professor Fernald’s interesting discussion of our eastern coastal 
species of Limosella reached me as I was on the point of taking 
up the same problem. I had suspected, and had tentatively so 
marked it in my notes, that our eastern species would prove 
distinct from L. tenuifolia Wolf of Europe, and should be called 
L. subulata Ives. That it was specifically distinct from the plant 
of the Rocky Mountains I was certain, having studied and made 
descriptions of both in their native environments. 

My notes, made from living plants and supplemented by 
herbarium study, show the following contrast between Limosella 
aquatica of the Central Rockies and nearby plains and L. subulata 
of the Atlantic seaboard: 

L. aquatica.—Corolla about 2 mm. wide; lobes somewhat 
spreading, acute or acutish, dull-white. Anthers about I mm. 
long, purplish. Capsules 2.5-3.2 mm. long, borne on spreading 
pedicels. Seeds .5 mm. long, dull amber-brown, about 6-7 
ridged, relatively coarsely transverse-lined. Calyx-lobes uni- 
form. Leaves about 3 cm. long, consisting of a petiole and a 
more or less dilated lanceolate blade about I cm. long. Plant 
rosulate, 10-20 leaved, surrounded by numerous radiating few- 
jointed stolons. 

L. subulata.—Corolla about 3 mm. wide; lobes widely spread- 
ing, obtuse, white, tinged with lavender-blue. Anthers about 
2 mm. long, dark purple-blue. Capsules 2—2.3 mm. long, borne 
on arcuately decurved pedicels. Seeds .6-.7 mm. long, bright 
amber-brown, about 8-9 ridged, more finely transverse-lined. 
Calyx-lobes upcurved, in fruit the tube tending to split on the 
anterior side. Leaves 1.5-2 cm. long, nearly filiform, terete, 
obtuse. Plant chain-like, consisting of plantlets borne on joints 
of extensively creeping filiform stolons, each plantlet usually 
5-10 leaved. 

In agreement with Professor Fernald, I am unable to distin- 
guish the plant of the Rockies from that of Eurasia. The 
western plant sometimes has pinkish corollas, but, so far as I can 


31 


find, variability of color between white and pink is characteristic 
of the European plant,* rather than a normal ‘pink or flesh- ~ 
color.” This species, Limosella aquatica, appears to be the most, 
cosmopolitan member of the Scrophulariaceae, and its simple 
flower-structure and acaulescent habit mark it as primitive. 
It occurs to-day upon all the continents, and is even credited to 
New Zealand. Whether eventual knowledge will show that it 
has held conservatively true throughout its supposed range may 
be doubted, but certain it is that deviations are mostly slight 
and remote. However in widely scattered parts of the earth 
it has “thrown ofi’’ suggestively parallel species. Thus Limosella 
subulata may be closely duplicated in the Vancouver Island 
region, and in Argentina—but a priori assumption would be that 
these are not identical with it. 

My field-acquaintance with Limosella subulata has been con- 
fined to one colony, but that fortunately extensive, growing 
about the margins of Old Sams Pond, Point Pleasant, New 
Jersey. This is a small pond of fresh water lying in the lea of 
the coast sand-dunes. The Garden herbarium shows a consid- 
erable series of specimens from sandy margins of such fresh sand- 
dune ponds, ranging from here northeastward to Nantucket. 
These plants are partially, though inconstantly recognizable, 
from the species of muddy saline tidal habitats by their pedicels 
being more recurving, their capsules blacker; their sepals more 


* The following quotations, chosen from various countries, confirm this: Baxter, 

Brit. Phan. Bot. pl. 212, “‘ pale rose-colored or white,”’ illustrated as white; Sowerby, 
.Engl. Bot. 5: pl. 357, “‘whitish without, red on the inside,’ illustrated as pink; 

Reichenbach, Ic. Fl. Germ. 20: 54. pl. 1722, “‘corolla albida; maculae brunneae sub 
basi cujusvis laciniae corollae, suppositae intus saltem maculae citrinae,”’ illustrated 
as described; Coste, Fl. France 3: 27, ‘‘blanches ou rosees’’; Murino, FI. Galicia 
too. “blanca’’; Schinz & Keller, Fl. Schweiz 456. ‘‘weisse od. rotlichweisse’’; 
Parlatore, Fl. Ital. 6: 546, ‘‘bianchiccio.” 

7 A letter from Mr. E. P. Bicknell, concerning Limosella on Nantucket, em- 
phasizes its occurrence about the sandy margins of ‘‘closed,’’ that ‘is completely 
land-locked ponds. Some of these are freshwater, but one is mentioned as probably 
at least partly brackish. He calls attention to the fact that in ponds which stretch 
some miles inland from the shore Limosella will occur only at the shoreward 
extremities. Specimens sent from the deeper water of certain ponds much exceed 
in length of leaves the dimensions of the key above, and in coarseness of growth are 
like the tide-water plant. The halophytism of Limosella subulata would make a 
valuable physiological study. 


32 


frequently obtuse, and the leaves more slender. If these modi- 
fications be wholly ecological, are they mainly a response to a 
sandy instead of mud substratum, or to the lack of salt, or in 
good part to freedom from periodic inundation? 

The range of Limosella subulata must be extended southward 
to Chesapeake Bay. G. H. Shull 306 is from the ‘northeast 
shore of Gunpowder River, one third mile northeast of its mouth,” 
Maryland, and certainly from between high and low tide. This 
collection and most of those from the tide-water of the Delaware 
River are of plants coarser, usually with longer and wider leaves, 
than the typical New England form. While the plant occurs 
on the Delaware between. Philadelphia and Trenton, as near 
Burlington, New Jersey, this is much above the usual limit of 
salt water. As a general statement, we may say that Limosella 
subulata is primarily a plant of brackish soil, but that it is fully 
able to meet a dilute or even quite non-saline environment. 


New YorK BOTANICAL GARDEN 


IN THE WAKE OF THE ENEMY! 


This dirge for the orchards of France may be familiar to many of our readers, 
but losses described by the letter immediately following the verse, are just as 
indefensible. Can there still be found in this country people who, in spite of acts 
like these, cherish pre-war delusion about the “‘ The Kindly German?’’—Ep. 


THE TREES OF FRANCE. 


Hush, little leaves, your springtime dance, 
Sigh for the murdered trees of France. 


Friends were they of the peasant folk, 
Friends whom the birds and kine bespoke. 


Spoil are they of destroying lust, 
‘Not of the battle stroke and thrust. 


They are a garden still: to see, 
They are the world’s Gethsemane. 


Hush, little leaves, your springtime dance, 
Sigh for the murdered trees of France. 
—McLandburgh Wilson. 


33 


(The following extract from a letter of M. Jules Cardot, the 
noted French bryologist of Charleville, France, was recently 
transmitted to me through M. Thériot, of Havre. I am sure 
that friends of M. Cardot will be glad to learn tidings of him. 
—E. B. Chamberlain.) 

“Depuis notre arrivée ici, je vis des jours qui compterons, 
certes, parmi les plus pénibles de ma vie, et si nous n’avions pas 
la victoire, qui nous console de tout, je me demande si je n’aurais 
pas été tenté d’en finir avec l’existance. Vous ne pouvez vous 
imaginer le spectacle que présente notre pauvre maison, l’état 
de saleté repoussante et de dévastation dans lequel elle se trouve. 
Partout des meubles brisés, les portraits de famille lacérés, des 
livres en lambeaux épars de la cave au grenier, les armoires, les 
secrétaires fracturés, quoique tous les clefs étaient sur les portes; 
tous les beaux meubles anciens disparus et remplacés par d’autres 
meubles qui ne nous appartiennent pas. Les livres qui n’ont 
pas été dechirés formaient dans le grenier une indescriptible 
salade; on se demande comment on peut arriver 4 mélanger 
ainsi une bibliothéque; ce doit étre un travail trés fatigant! 
A cété de cela des choses déconcertantes. Mes collections qui 
on avait dites évacuées sont la, en partie du moins. Je les a’ 
retrouvées, entassées dans le fond du grenier et recouvertes par 
ma bibliothéque scientifique, qu’on a jetée péle-méle par dessus. 
Malheureusement mes pauvres collections sont loin d’étre au 
complet. Il manque, outre tous les matériaux non étudiés, une 
énorme collection du Japon, de plus de 5,000 N°, contenant des 
centaines d’espéces nouvelles, une collection de Juan Fernandez, 
une autre des iles Sandevich et une autre encore de Saghaline, 
tout cela probablement détruit et perdu sans retour.’” 


PROCEEDINGS OF THE CLUB 
NOVEMBER 27, 1918 


The meeting was held in the Morphological Laboratory of the 
New York Botanical Garden at 3:30 P.M., with Vice-President 
- Barnhart in the chair. There were twelve persons present. 


b4 


The minutes of October 30 and November 12 were read and 
approved. 

The nomination and election of Bro. M. Victorin, Longueiul 
College, Quebec, Canada, followed. 

The announced scientific program was then in order. Dr. 
P. A. Rydberg read a paper on ‘‘The Distribution of the Montane 
Plants of the Rocky Mountains.’ This paper will be published 
in the Bulletin of the Club. 


Meeting adjourned. 
B. O. DoDGE, 


Secretary 
DECEMBER 10, 1918 


The meeting was held at the American Museum of Natural 
History at 8:15 P.M. President Richards occupied the chair. 
There were twenty eight persons present. The minutes of 
November 27 were read and approved. 

The nomination and election of Dr. George E. Nichols, Yale 
University, and President R. B. von Kleinsmid, University of 
Arizona, Tucson, followed. No other business was transacted. 

The announced scientific program consisted of an illustrated 
lecture on ‘‘The Botanical Gardens at Buitenzorg, Java,” by 
Dr. H. A. Gleason. 


Adjournment followed. 
B. O. DopGE, 


Secretary 


THE PLANTING OF TREES AS WAR MEMORIALS* 


At the annual meeting of the Managers of the New York 
Botanical Garden on January 13, 1919, the following suggestions 
by Mr. Edward D. Adams were approved and ordered printed: 

At this time, when permanent memorials to the defenders of 
our flag by land and sea are being considered throughout our 
land, and projects for community: monuments of various designs 
are planned, we venture the suggestion that individual, as well as 
associated, action can effectively and economically be taken in 


* Reprinted from the JouRNAL OF THE NEW YoRK BOTANICAL GARDEN, 20: 
I-2, Jan., 1919. 


35 


honor of all who have served or of those who have made the 
supreme sacrifice, by planting memorial trees. 

Such trees may properly be planted in the front yard, on the 
street, at the home entrance, in a park, as the decoration of an 
avenue, in single specimens or in groups of different species for 
artistic effects of form and color. 

As representing sentiments to be long cherished, such me- 
morials would be tenderly cultivated and protected. 

Their shade and fruit would yield comfort and satisfaction. 
Their growth would add value to the home and become an asset 
that succeeding generations would inherit. . 

Naturally, only those trees should be selected for memorials 
to family, school, church, and municipal honor, that will grow 
best in each locality and of those species that will be appreciated 
for their beauty, grandeur, long life, and utility. 

The number of kinds of -trees suitable for memorial planting 
is large. The widely different climates of different parts of the 
United States require the selection of such kinds as will grow 
vigorously, and the character of the soil should also be taken 
into consideration; such information to those not versed in tree 
planting can usually be had from the nearest nurseryman or from 
officials of the Agricultural Experiment Station. 

Those who live in homes without available grounds for plant- 
ing, might contribute to the cost of a tree for its planting as 
part of a memorial grove in a park or garden. 

The selection of the tree, the preparation of the location, and 
the design of the label or honor roll, may be considered and car- 
ried out in family conferences and with the participation of each 
member. 

These preparations should be made as our men return, so that 
the signing of the treaty of peace may be celebrated over the 
nation wide by the simultaneous planting of the honor tree of 
each family and community that has cherished a service flag in 
the period of our war. 

At the New York Botanical Garden, a war memorial planta- 
tion of Douglas Spruce, a characteristic American evergreen 
tree, will be established this spring; about one hundred trees 


36 


five feet high having been secured for this purpose. For those 
who do not have land available and who would like to have a 
memorial tree planted, the offer is made to designate one of 
these spruces as desired on receipt of ten dollars, which will cover 
cost of tree, of planting, and of its care, which will be the same 
as that of other trees in the Garden. 


NEWS ITEMS 


Professor Henry Allan Gleason, of the University of Michigan, 
recently spent two months in the study of North American Iron- 
weeds, the genus Veronia and near allies at the New York 
Botanical Garden. Professor Gleason published some years ago 
a preliminary revision of Vernonia and he is now preparing the 
manuscript of the tribe Vernonieae for the North American Flora. 
Dr. Gleason spent a day at the Brooklyn Botanic Garden, where 
he revised the collection of Vernonia in the herbarium of that 
institution. 


Mr. Charles Piper Smith, who has published several papers on 
Lupinus in the Bulletin, spent ten days recently in studying 
these plants at the herbarium of the Brooklyn Botanic Garden, 
and at the Gray Herbarium, Cambridge. 


We learn from the Michigan Agricultural College Record of 
the death on December 6 of Miss Rose M. Taylor, instructor in 
botany at the College. 


We learn from the Evening Sun that because of the similarity 
of climate and soil conditions of Texas and the land upon which 
the Jewish ‘‘ Republic of Judea ”’ will be built, the Zionist Society 
has retained Dr. J. J. Taubenhaus, plant pathologist of the 
Texas agricultural experiment station, for a high agricultural 
post in the new nation. 

Much of the data compiled during his service here will be 
available for use in Palestine, Dr. Taubenhaus says. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of TorREYA in which their papers appear, will kindly notify the 
editor when returning proof. 

Reprints should be ordered, when galley proof is returned to the editor. . The 
New Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
following rates: 


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Covers: 25 for $1.00, additional covers 114 cents each. 
Plates for reprints, 50 cents each per 100. 


Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs. E. G. BRITTON, Chairman. 
J. H. BARNHART, Pror, JEAN BROADHURST 
Miss C. C. HAYNES B. O. DODGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F,. J. SEAVER 
J. H. BARNHART, Chairman. Membership Committee 
R. A. HARPER J. K. SMALL, Chairman. 
N. L. BRITTON T. E, Hazen 
A. W: Evans E. W. OLIVE 
M. A. Howe Local Flora Committee 
H. H. RussBy N. L. Britton, Chairman. 
Field Committee _ Phanerogams: Cryptogams: 
F. W. PENNELL, Chairman. E. P. BICKNELL Mrs. E.G. BRITTON 
“Mrs. L. M. KEELER N. L. BRITTON T. E. HAzEN 
MICHAEL LEVINE C.-C, Curtis M. A. Howe 
GEORGE T. HASTINGS K. K. MACKENZIE MICHAEL LE VINE 
PrERcy WILSON NORMAN TAYLOR W. A: MuRRILL 


F, J. SEAVER 
Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton AS Sphaeriaceae, Dothideaceae: H. M 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae; M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M. Richards, - F. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
; Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes:'A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurst 


Discomycetes: B. O. Dodge Insect galis: Mel T. Cook 


OTHER PUBLICATIONS 


OF THE 


TORREY BOTANICAL CLUB 


(1) BOLLETIN | 


_ A-monthly journal devoted to general botany, established 
1870. Vol. 45 published in 1918, contained 519 pages of text 
and 15 full-page plates. Price $4.00 per annum. For Europe,. 
18 shillings. Dulau & Co.,. 47 Soho Square, London, are, 
~agents for England. 

Of former volumes, only 24-45 can be supplied entire ; cer- 
tain numbers of other volumes are available, but the entire stock 
of some numbers has been reserved for the completion of sets 
Vols. 24-27 are furnished at the published price of two dollars 
each ; Vols. 28-45 three dollars each. : 

Single copies (30 cents) will be furnished only when not 
breaking complete volumes. RL 


(2) MEMOIRS 


The Memoirs, established 1889, are published at irregu-— 
lar intervals. Volumes’ 1-15-are now completed; No. 1 of 
Vol. 16 has been issued. The subscription price is fixed at 
$3.00 per volume in advance; Vol. 17, containing Proceedings 
of the Semi-Centennial Anniversary of the Club, 490 pages, was 
issued in 1918, price $5.00. Certain numbers can also be pur- 
chased singly. A list of titles of the individual ae and of 
prices will be furnished on application. 


(3) The Preliminary Catalogue of Anthophyta and Pteri- | 
dophyta reported as growing within one hundred miles of New 
York, 1888. Price, $1.00. 


Correspondence relating to the above publications should be 
addressed to 
DR. BERNARD O. DODGE 
Columbia University 


New York City 


Vol. 19 March, IgIg No. 3 


PTORREYA ~ 


A Monruiy Journar or BoranicaLt Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


“JOHN TORREY, 1796-1873. 


CONTENTS 
The Japanese Honeysuckle in the Eastern United States: E. F. ANDREWS..........- 37 
Variations in the flowers of Erythronium Propullans Gray: C. O. ROSENDAHL..... 43 
New names for species of Phanerogams: J. C. ARTHUR. .:1.0c00c060 cesssetsseseeenveeeees 48 
Per VOlOvical NOtES: A. LEROY ANDREWS ..5 /c-die sie 90h vdovuysoncsurdenenhiadn cadven Secale op¥cbe 49 
DAGtES- ANG NEWS. silos ce scs shove subepenegtem isvaderdves SUR TR UTE yak Saeki NOR (oi Gr papa aera 51 


PUBLISHED FOR THE CLUB 


At 41 NortH Queen Street, LANcAsTER, Pa. 
BY THe New Era Printinc Company 
"Entered at the Post Office at Lancaster, Pa,, as second-class matter. 


THE TORREY BOTANICAL CLUB 


OFFICERS, FOR 1919 


President 
H. M. RICHARDS, Sc.D. 


Vice- Presidents. 
JOHN HENDLEY BARNHART, A.M., M.D 
C. STUART GAGER, Pu.D. 


Secretary and Treasurer 
BERNARD. O. DODGE, PH.D. 
COLUMBIA UNIVERSITY, N. Y. City. 


Editor 
ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


JEAN BROADHURST, Pu.D. M. LEVINE, Pu.D. 
J. A. HARRIS, Pu.D. ‘G. E. NICHOLS, PH.D. 
MARSHALL AVERY HOWE, Pu.D. . ARLOW B. STOUT, Px.D: 


NORMAN TAYLOR. 


Delegate to the Council of the New. York Academy of Sciences 
M. A. HOW®, PH.D. 


OFFICIAL ORGAN OF THE WILD FLOWER PRESERVATION 


SOCIETY OF AMERICA. 


 Torreya is furnished to subscribers in the United States and 
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NORMAN TAYLOR 


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IJids 


werwe ae 


TORREYA 


Vol. Ig No. 3 
March, IgIg 


THE JAPANESE HONEYSUCKLE IN THE EASTERN 
UNITED STATES. 


By E. F. ANDREWS 


The rapidity with which introduced weeds can multiply and 
take possession of new territory has been repeatedly demon- 
strated by such examples as the Russian thistle (Salsola pestifer), 
bitterweed (Heleniwm tenutfolium) and the Sida (S. Spinosa and 
S. rhombifolia)—plants which have become such common pests 
in certain parts of our country. As a general thing these un- 
welcome intruders belong to the class of herbaceous annuals and 
biennials, whose frequent succession of new generations, with 
the opportunities for seed production and distribution which 
this affords, makes them much more efficient travelers than the 
slower-growing woody shrubs and vines. 

A notable exception to this rule, however, is furnished by the 
Japan honeysuckle (Lonicera japonica), an exotic from Asia, 
which I remember to have known in my youth only as a care- 
fully cultivated and highly prized ornamental plant, twining 
about the piazzas of the old plantation mansions and covering 
the “‘summer houses’’—pergolas, they would be called now—in 
old-fashioned southern gardens. The flowers are very fragrant 
and showy, and it was a profuse bloomer under cultivation, but 
since it has run wild and taken on the weedy habit, it has to a 
large extent given up flowering, and propagates chiefly by vege- 
tative means. Wherever a shoot touches the ground it strikes 
root and then sends forth a numerous progeny of young shoots 
to repeat the process. The prostrate stems and those in con- 
tact with the soil, even on high banks and ledges, where there 


[No. 2, Vol. 19 of ToRREYA, comprising pp. 21-36, was issued 19 March, 1919.] 


37 


38 


is plenty of light, never, or very rarely produce flowers, but ex- 
pend their surplus energy in adding to the network of tangled 
cords that covers the ground wherever this ruthless invader gets 
a foot hold. It will climb as high as heaven if it can find any- 
thing to lean on, converting the wooded areas in the moist river 
bottoms into an impenetrable jungle with its tangled cords of 
interlacing vines; or if forced to accept an humbler position, 
crawling with equal facility over the gullied slopes of arid hill- 


Fic. 1.—Japanese honeysuckle covering the side of a railroad cut near Rome, 
Ga. The white patches in the foreground are not snow, but naked portions of 
the very sterile yellow clay soil. 


sides or along the borders of dusty roads. This faculty might 
be turned to good account in stopping washes and covering un- 
sightly clay banks, though its utility for such purposes seems never 
to have been tested. But while accommodating itself readily to 
almost any conditions, it shows a marked preference for moist 
woodlands and the borders of streams, and as its presence in 
such places does not interfere with the crops, or threaten any 
direct pecuniary loss, it has not attracted the attention of either 
the economist or the agriculturist. 


39 


But to the botanist engaged in any kind of field work this for- 
eign immigrant is a most undesirable accession to our plant pop- 
ulation. It infests his favorite hunting grounds and besets his 
steps with a tanglefoot of snares even more exasperating than 
the barbed wire fences, sometimes forcing him—and more espe- 
cially hery—to cut short such explorations. But the chief indict- 
ment against it is the ruthlessness with which it is overrunning 
and destroying our native plants wherever it comes in competi- 
tion with them; and it is no uncommon thing to see acres upon 
acres of brushwood and haw thickets, sometimes including trees 
of considerable size, buried under the rank growth of this ag- 
gressive invader. As it has no way of climbing except by coiling 
around a support, which is a rather tedious process in the case 
of large stems; it can reach the crown of high-branching trees 
only by climbing upon the under brush of shrubs and young 
shoots until it comes in contact with some overhanging bough— 
and then it has a free right-of-way. It also utilizes the stems and 
branches of other climbers that have already made good their 
ascent—trumpet vine, catbriars, grape, Virginia creeper, and the 
like, not excepting those of its own kind. As the stems of both 
the twiner and its support grow larger, the tension often becomes 
so great that the coils are tightened like a noose, and become so 
deeply imbedded in the supporting stem as to give it the appear- 
ance of a huge corkscrew, and unless themselves broken or loos- 
ened by the strain, may cause the death of the parts above. 
More frequently however, it kills by smothering its victims under 
a dense network of interlacing cords, commonly from 3 to 6 mm. 
thick, loosely twisted together. I have counted as many as 27 
strands of all sizes, from I to 10 mm. thick, twined into one of 
these living ropes. A single stem is rarely more than 1 or 2 cm. 
(about 34 of an inch) thick, though in one instance I have seen 
a single honeysuckle vine 18 cm. (7 in.) in girth, smothering a 
wild plum tree (P. nigra) 1.5 dm. (6 in.) in diameter. It began 
by gripping a shoot from the base of the plum, in a spiral of 4 
rings which have been drawn so tight by the continued growth 
of both stems that the honeysuckle, the more elastic of the two, 
has been flattened out like a piece of tape. As for the plum 


40 


shoot, it is now dead, and from the end of the stub the climber has 
reached out to the main stem and spread over the crown a net- 
work of luxuriant branches under which the tree is being slowly 
smothered to death. 

This sort of piracy is no uncommon thing in the vegetable 
world, any more than in our own, but what surprised me in this 
case was the unusual size of the climbing stem. I took it fora 
grape vine at first, as the bark is fibrous like that of the grape, 
and it was not until I had plucked off leafy twigs actually grow- 
ing out of it that I could feel sure they really belonged there and 
were not merely ‘“‘hangers-on”’ of a hanger on. The bark’ is of 
a lighter color and softer texture than that of the grape, and 
also more easily detached. 

On this lusty vine only one fowenne& sprig, with but two ber- 
ries, wasfound. This was on November 7, 1917, and is the second 
specimen of fruit recorded in my notes for that year, though 
others may have been observed without being mentioned, and 
others still may have escaped notice on account of the difficulty 
of distinguishing them among the dark, evergreen foliage. But 
while all this may be so, I have kept up such a constant lookout 
for the fruiting sprays, and their scarcity is the subject of such 
frequent comment in my notes that although their presence may 
sometimes be overlooked, this is not a satisfactory explanation, 
and the fact remains that the production of fruit (and conse- 
quently of seed) is much less than would be expected of so pro- 
lific a stock. But while the flowers appear to be highly special- 
ized for insect pollination, they seem, in the wild state, to 
have no set time for blooming. Even in spring it is unusual to 
see a honeysuckle vine loaded with flowers like the jessamines 
and clematis, but it continues to blossom sporadically throughout 
the greater part of the year (in this latitude, from April to De- 
cember) producing a few sprays here and there—hardly more in 
May than in October. In this way, many of the late bloomers 
may ‘‘waste their sweetness on the desert air” so far as pollin- 
ation and the perfecting of fruit is concerned. 

But the most puzzling thing about this successful invader is 
how it has managed, with such imperfect provision for transpor- 


41 


tation over long distances, to spread over so vast a territory ~ 
within the memory of persons still living. No mention is made 
of it in either ‘‘Chapman’s Flora of the Southern States”’ (1884) 
or in the VIth edition of Gray's Manual (1889), and it was not 
until about this period that my own attention was aroused by 
the discovery that it was beginning to run wild in low, damp 
places around Macon, Ga. Since then it has spread over prac- 
tically the whole of the Eastern States, from the Gulf of Mexico 
to the estuary of the Hudson, making itself equally at home in 
the low hammocks of the Coastal Plain, on the old red hills of 
the Piedmont region, on the stony ramparts of the Lookout 
Plateau, and onward for a thousand miles up the great Appa- 
lachian Valley. A writer from Texas in the American Botanist 
(Vol. 24, p. 5) mentions it as having “established itself in the 
brush around dwellings’’ in some parts of that State, and Dr. 
R. M. Harper also writes me that he has seen it growing along 
roadsides in Hingham, Mass. 

The ease with which it propagates by runners will account for 
the rapid dispersal of the species locally, but for those distant 
migrations by which it has spread from Texas to New England 
and from the mountains to the sea, some more expeditious means 
of transportation is needed. The dissemination of seed through 
the agency of birds is the most natural means that suggests it- 
self, and is probably the one employed, though the adaptation 
for this purpose is not very apparent. The berries, in addition 
to their infrequency, are “‘conspicuously’’ inconspicuous, being 
small, black, and sessile, or nearly so, in the axils of the dark green 
leaves, where it is difficult to see how they could attract atten- 
”’ The small nutlets are 
embedded in a mucilaginous pulp like that of the mistletoe, but 
of a dark greenish color and an insipid, bittersweet taste, that 
would not seem likely to tempt a fastidious palate. It is not 
unlikely, however, that this pulp may play an important part 
in the distribution of seed, by sticking to the feet of birds and 
insects, and being carried about from place to place like the 
mistletoe. The plant is spread to some extent, even locally, by 
seed, and I have occasionally found a new colony forming in 


tion even in a real “‘bird’s-eye view. 


42 


places 200 meters (about 620 ft.) or more, from any others of 
the species which could have given rise to it. The seedling starts 
by sending out a number of prostrate branches which creep along 
on the ground sending out runners of their own in every direc- 
tion until they find something to climb on, and in an incredibly 
short time will overrun everything that stands in their way. 


Fic. 2—A honeysuckle jungle on the borders of a small stream in Wilkes 
County, Ga. 


But after all has been said, the paucity of fruit in a plant so 
widely distributed has always been a puzzle to me, and as the 
flowers are dependent upon insect fertilization, I have some- 
times wondered whether this might not be a case like that of the 
Smyrna figs, in which a particular insect partner was needed to 
insure pollination. The most reasonable explanation, however, 
seems to be that wherever the honeysuckle can propagate itself 
vegetatively, it employs that method in preference to wasting 
its energies in the more exhausting and expensive process of seed 


43 


production. In other words, nature, here, is economizing effort 
and following the line of least resistance. This accords with the 
fact that prostrate and low climbing branches do not bloom and 
that fruit and flowers are found only in positions where the op- 
portunity for vegetative multiplication is restricted or wanting. 
In fact, the most remarkable crop of both fruit and flowers that 
I remember ever to have seen, was on a vine climbing over a 
wire fence between a cotton field and a potato patch, where the 
farmers were giving it such a hard fight that it had no chance 
to spread over the ground and was obliged to find some other 


outlet for its vital energy. 
ROME, GEORGIA 


VARIATIONS IN THE FLOWERS OF ERYTHRONIUM 
PROPULLANS GRAY 


By C. O. ROSENDAHL 


Several species of the genus Erythronium are characterized by 
certain structural peculiarities of the flowers chief of which is 
the marked heteromorphism of the stamens. This has been dem- 
onstrated in two of our common eastern species, E. albidum and 
E. americanum by Meads* and Grafff and in a number of west- 
ern and mid-western species by Pickett.f Among those studied 
by Pickett is E. propullans, a somewhat peculiar species which, 
so far as definitely known, is limited in its distribution to a small 
geographical area of southeastern Minnesota. In this restricted 
area it has been found only in a few places in the valleys of the 
Cannon and the Zumbro rivers, where it grows on wooded, allu- 
vial bottomlands. 

Asa result of the very limited distribution of the species there 
are comparatively few specimens of E. propullans in the herbaria 
of the country and Pickett states that his observations on it were 

* Meads, M.E. The Range of Variation in Species of Erythronium. Botanical 
Gazette 18: 134-138. 1893. 

+ Graff, Paul W. The Stamens in Erythronium Americanum. Torreya 16: 
180-182. I9106. 


i Pickett, F. L. The length of Erythronium Stamens. Torreya 17: 58-60. 
TOU: 


44 


confined to only a few plants. He makes the suggestion that it 
would be desirable to examine more extensive collections to see 
if stamen dimorphism is characteristic of the species and accord- 
ingly the writer made it a point to look over the specimens of 
it in the herbarium of the University of Minnesota to see if ad- 
ditional proof could be obtained. The observations on the 
herbarium material were supplemented by a study of numerous 
specimens in the field in May, 1918. 

These observations show beyond any doubt that the stamens 
of Erythronium propullans, like those of several other species of 
the genus, are characteristically heteromorphic. In fact there is 
perhaps an even greater proportional difference in the lengths of 
the two sets of stamens than is found in the other species, for in 
E. propullans the outer whorl of stamens reaches scarcely above 
the base of the anthers of the inner set. The accompanying 
stereoscopic photographs, which were made with a Zeiss stereo- 
scopic camera with regular binocular objectives and with the 
flowers. immersed in water, show this fact clearly. (The value of 
the figures is enhanced by examining them through an ordinary 
stereoscope.) 

In the field material the average length of the outer stamens 
is 6.32 mm. while that of the inner is 7.99 mm., a difference of 
1.67 mm. There is considerable variation in the size of the 
anthers ranging from I.9 mm. to 3.5 mm. in length. The aver- 
age length is about 2.46 mm. In some flowers the anthers of 
the outer stamens are regularly about .5 mm. shorter than those 
of the inner but this is not generally the rule and many cases 
were noted in which the anthers of the inner stamens were smaller 
in size than the outer. For the most part the anthers of one 
whorl of stamens differ as much from one another in size as they 
differ from those of the alternating whorl. This marked ten- 
dency to variation in the length of the anthers does not seem to 
affect the filaments for in all flowers examined the outer filaments 
were found to be constantly and uniformly shorter than the inner 
ones. 

While examining the flowers for stamen heteromorphism an- 
other feature was brought to light which apparently has hitherto 


Fic. 1.—A flower of Erythronium propullans with four perianth segments and 


four stamens, showing the pronounced difference in the lengths of the two sets of 
stamens. Fig. 2. A flower with five perianth segments and five stamens, two of 
which are long and-three short. Fig. 3. Three plants of E. propullans showing 
flowers with four, five and six perianth segments. On two of the plants the 


young offshoot can be distinctly seen. 


46 


been overlooked in E. propullans, namely a remarkable varia- 
bility with regard to the number of the perianth segments, © 
stamens and carpels. 

Of a total number of 51 flowers examined in detail only six had 
six complete or normal perianth segments and only three of 
these had the full complement of stamens. Three flowers had 
five normal perianth segments and one of reduced size. There 
were eleven flowers with five perianth segments and twelve with 
five stamens. By far the largest number of flowers, namely 
thirty-one, had four perianth segments and there was a total of 
thirty-four which had only four stamens. One flower had three 
stamens and another one had only two. The following tabu- 
lation shows the variations in a more graphic way: 


No. of perianth seg- 2 | 


INCHES HAs tae < ox = 6 | 5 -+ I ab- 
normal 5 4} No. of stamens. 6 5 | 4Szeuae 
No. of flowers...... 6 3 TET || Bi 2) 121/370 erase 


It is thus obvious that only about I2 per cent. of the flowers 
possess the full number of perianth parts and only about 6 per 
cent. the full number of stamens. On the other hand about 61 
per cent. of the flowers have only four perianth segments and 
fully 67 per cent. have only four stamens. About 21 per cent. 
of the flowers have five perianth parts and 23 per cent. have five 
stamens. Where there are only four perianth segments and four 
stamens each series is arranged in two alternating whorls of 
two each, the two shorter stamens occupying the outer whorl. 
In most cases where five perianth segments and five stamens are 
present the suppression has occurred in the inner whorl of the 
two respective series, thus leaving three short stamens and two 
long (Fig. 2). In at least one case the reverse condition with re- 
gard to the stamens was observed. 

In the typically trimerous flowers the ovary is 3-celled but in 
the flowers having only four perianth parts and four stamens the 
pistil is reduced to two carpels and the ovary is 2-celled. In the 
flowers with five perianth parts and generally five stamens the 
pistil is usually made up of three carpels with three cells in the 


47 


ovary but sometimes one of the carpels is only partially devel- 
oped, resulting in a somewhat irregular stigma and only two 
complete cells. In one case a flower with two separate pistils 
was observed. The pistil, however, shows the least variation in 
size of all the organs of the flower of E. propullans, the style being 
uniformly 5 mm. in length and the ovary about 3 mm. when the 
flowers are in anthesis. 

So far as the writer is aware the flowers of E. propullans are 
considerably smaller than in any other species of the genus. 
They vary in length from 9 to 13 millimeters but the majority 
are a little over 10 mm. long. Attempts to ascribe to other 
factors than heredity the difference in the size of flowers of var- 
ious related species of a genus are mostly futile, yet the hypothe- 
sis put forth by Blodgett* in explanation of the reduction in the 
size of the flowers of E. propullans seems to the present writer 
at least very plausible. 

As is well known the offshoot in E. propullans pushes out from 
the stem near the middle (Fig. 3), its bud originating “‘at the 
base of the peduncle in the axil of one of the leaves.’’ Thus the 
“‘vascular system of the peduncle supplies, through branches, 
the necessary strands for the offshoot.’”’ This side-tracking of a 
considerable amount of the food supply going up the peduncle 
may have had, in the opinion of Blodgett, ‘‘considerable influ- 
ence in the reduction in size noticeable in the flowers of this form 
in contrast to the rest of the genus.” 

It seems very probable that the prevalent reduction in the 
number of the floral organs is due to the same cause and we have, 
at least in this species, a very simple physiological explanation 
for the fluctuations in the floral structures. 

In conclusion it is worth noting that the genus Erythronium 
belongs to a subfamily of the Liliaceae in which the trimerous 
plan of the flower is quite consistently adhered to. The char- 
acteristic variations in the number of the perianth segments, 
stamens, and carpels and especially the preponderance of dimer- 
ous flowers in E. propullans are therefore very striking. 


* Blodgett, F. H.. The Stem Offshoot in Erythronium propullans Gray. Johns 
Hopkins University Circular, 3-5. June, 1909. 


48 


NEW NAMES FOR SPECIES OF PHANEROGAMS 
By J. C. ARTHUR 


While studying the Uredinales and listing their hosts for pre- 
sentation in the North American Flora a number of phanero- 
gamic species have been encountered, which have not been trans- 
ferred, so far as the writer can ascertain, to the genera under 
which related species are being listed. As it is desirable to have 
these transfers made for the sake of uniformity, and as no one 
else seems desirous of making them at this time, they are here 
recorded. The advice of Mrs. Agnes Chase, Mr. Percy Wilson 
and Dr. F. W. Pennell has been followed, although the writer 
is to be held responsible for any errors that may occur. 

Senites Hartwegi (Fourn.) nom. nov. (Zeugites Hartwegi Fourn. 
Mex. Pl. 121. 1886). A grass of Central America, and known 
from Mexico by the type specimen only, Hartweg 569. It bears 
Uredo Zeugitis Arth. & Holw. from San Rafael, Guatemala, 
7000 feet alt. (Am. Jour. Bot. 5: 538. 1918). 

Sanguinale pruriens (Trin.) nom. nov. (Panicum pruriens Trin. 
Gram. Pan. 77. 1826). A grass of Hawaii, that has been re- 
ferred to Panicum sanguinale. Professor A. S. Hitchcock holds 
it to be clearly distinct. He observed in the field that the racemes 
are erect, not spreading as in P. sanguinale, and Mrs. Chase has 
found that the first glume is wanting and the second very minute. 
It bears Puccinia oahuensis Ellis & Ev., which was only known 
from the type collection. obtained on the slopes of Makiki, Is- 
land of Oahu, by A. A. Heller, in 1895, until it was detected by 
Mrs. Chase on two collections of the grass made near Honolulu 
by Prof. Hitchcock, one along a ditch, June 16, 1916, no. 73735, 
and the other as a weed in shady places, Halfway House, Mt. 
Tautalus, June 24, 1916, no. 13862. Puccinia oahuensis is 
scarcely distinguishable morphologically from P. substriata Ellis 
& Barth. 

Nymphoides Grayanam (Griseb.) nom. nov. (Limnanthemum 
Grayanum Griseb. Cat. Pl. Cub. 181. 1866). A West Indian 
aquatic plant in*the family Menyanthaceae, on which aecia of 
Puccinia Scirpi DC. were found in Cuba by Charles Wright in 


49 


1858. It still remains the only rust collection on this genus of 
hosts known for America. 

y Aureolaria virginica (L.) nom. nov. (Rhinanthus virginicus L. 
Sp. Plant. 603. 1753; Dasystoma virginica Britton, Mem. Torrey 
Club 5: 295. 1894). A common Scrophulariaceous plant of the 
northeastern United States, which bears aecia of Puccinia An- 
dropogonis Schw. 

Dasystephana spathacea (H.B.K.) nom. nov. (Gentiana spath- 
acea H.B.K. Nov. Gen. Sp. Plant. 3: 173. 1818). A Mexican 
species, which bears the widely distributed rust Puccinia Gen- 
tianae Link. 

Dasystephana Menzesii (Griseb.) nom. nov. (Gentiana Men- 
zestt Griseb. Gen. Sp. Gent. 292. 1839). A Californian species, 


which bears the rust Puccinia Gentianae Link. 
PURDUE UNIVERSITY, 
LAFAYETTE, IND. 


v 


BRYOLOGICAL NOTES 


V. Scapania nimbosa FROM NORWAY 
By A. LERoy ANDREWS 


Of the remarkable “Atlantic species’? of the northwestern 
European coasts washed by the Gulf Stream, obviously relicts 
of an older flora, two Scapanias stand out sharply from their con- 
geners. The one of wider distribution, commonly known as 
Scapania planifolia (Hook.) Dum., should according to Pearson 
bear the earlier specific name S. ornithopodioides (Dill.) Pears. 
It is known from various stations on the west coasts of the Brit- 
ish Islands, from the Faroes and a few localities on the west 
coast of Norway. According to Miiller* it is certainly identical 
with species known from isolated stations in Hawaii and the 
Himalayan region of India.— S. nimbosa Tayl. was hitherto 
known only from relatively few places on the western coasts of 
the British Islands. 

* Rabenhorst, Kryptogamenflora, VI, 521. 1915. The author’s earlier (1905) 
monograph of Scapania is not at present accessible to me. 


+ This conclusion is also accepted by Stephani, Spceies Hepaticarum, IV, 136f. 
1910. 


50 


In the summer of 1907 the Norwegian bryologist, Herr B. 
Kaalaas, kindly permitted me to accompany him on a collecting 
trip on the western Norwegian coast in Romsdals Amt. His 
main purpose was to establish more definitely the northern limit 
of the Norwegian range of the ‘‘Atlantic species,” many of which 
he had himself been the first to find in that country. While I 
was with him we found one new station for S. plantfolia, by the 
lake Gusdalsvand in Vanelven, a point which we reached from 
temporary headquarters at Aaeim. Our most northerly oper- 
ations, and the last before I was obliged to leave, began with a 
trip by water from Molde to the small fishing village on the low 
cape Bud. From there we walked to the little settlement of 
Farstad, as I remember, where we succeeded in finding quarters. 
It was Herr Kaalaas’ idea to investigate from here particularly 
the high promontory of Stemshesten. We learned, however, of 
an area of limestone to the southward in the Tverfjeldene* and 
decided to divide our forces for the one day we had available, 
Herr Kaalaas investigating Stemshesten, while I tried to reach 
the marble of the Tverfjeldene. With the time consumed in 
going and coming, together with a certain amount of climbing, 
I was not able to make a thorough survey of the place, but did 
find a number of interesting bryophytes. Among them was a 
Scapania which I took from its general appearance to be S. 
planifolia, and it was so recorded by Kaalaas as the most north- 
erly station for this species.t Miillert also records this as the 
northern limit of the species. On more careful examination my 
specimen proves, however, to be S. nimbosa. The descriptions 
of Macvicar§ with figures show two quite distinct species, and 
I have also been able to compare authentic material of both dis- 
tributed by the English hepaticologist, W. H. Pearson, so that 
there is no question as to the identity of the plant. The record 

* The gneiss of western Norway is varied by occasional outcrops of limestone 
(marble), which are in some cases large enough to support a distinctive calcicolous 
flora. We had previously driven from Molde to such a locality north of there con- 
taining a cave (Troldkirken), from which the Tverfjeldene are not far distant. 

+ Lat. 62° 56’ N. Untersuchungen iiber die Bryophyten in Romsdals Amt, 26- 
IQII. 


t Loe. cit. 
§ Handbook of British Hepatics, 368f. 1912. 


51 
represents a considerable extension of the limited range of S. 
nimbosa, which had been known only from the British Islands, 
and at the same time adds one to the list of ‘Atlantic species” 
known from Norway. 


ITHacA, N. Y. 


NOTES AND NEWS 


Dr. W. A. Cannon, of the staff of the Department of Botanical 
Research of the Carnegie Institution, reached San Francisco in 
the last week of April after an extended trip to Australia for the 
prosecution of his work on the root systems of desert plants. 


A specimen of Panicum urvilleanum Kunth in the National 
Herbarium collected by W. L. Jepson (no. 6049) near Edom in 
the Colorado Desert, southern California, shows several spike- 
lets bearing two sterile florets below the well-developed fertile 
floret. The florets resemble each other as to pubescence. The 
upper of the two is slightly longer and less pointed than the lower 
and has a well-developed palea. In the lower no palea has been 
observed, the lemma only being present. Sixteen other speci- 
mens from North and South America in the National Herbarium 
have been examined but in all the spikelets appear to be normal. 
So far as known this is the only species of Panicum showing a 
departure from the single sterile (or staminate) floret, character- 
istic of the tribe Paniceae. In Lasiacis anomala of the same tribe 
recently described* the spikelets normally bear two sterile florets, 
this being the first case known of the presence of a second sterile 
floret in any member of the Paniceae. In Panicum amalurum 
Hitche. & Chase and in species of Ichnanthus the glumes are 
sometimes multiplied but in these there is no fertile floret, a 
terminal staminate floret only being present——KATHARINE D. 
KIMBALL, Bureau of Plant Industry, U.S. Dept. Agric. 


The New York Botanical Garden is at present engaged in the 
preparation of a descriptive guide to the collections in the eco- 
nomic museum. In the course of its preparation, we have found 
so many omissions of common and important articles that we are 


* See Hitchcock, Journ. Washington Acad. Sci. 9:35. 1919. 


52 


making a special effort to complete the list before printing the 
Guide. It would be a great favor if readers of TORREYA would 
either collect for us such of our desiderata as may occur in their 
respective localities or notify us where they can be obtained. 

The following are desired for preservation in the fresh state 
in a mixture of one part of formalin to sixteen of water. They 
may either be placed in the solution at once, in ordinary fruit 
jars with the tops securely screwed down, and suitably labeled 
with name, locality, date and name of collector, or they may be 
sent to us wrapped in paraffin paper, provided they can arrive 
in a fresh condition. 

Wild leek (Allium tricoccum) plants bearing their bulbs. 

All wild gooseberries. 

Wild red currant. 

The sand blackberry. 

Vanilla grass (Savastana odorata). 

Sorghum cane, sugar and molasses. 

All huckleberries and blue berries of the south and south- 

eastern states. 

Mitchella repens in fruit. 

Chiogenes in fruit. 

Wild cranberry in fruit. 

Batodendron arboreum in fruit. 

Ripe olives on the branch. 

Yucca baccata fruit. 

Chinquapin twigs with ripe burs. 

Wintergreen berries on the stem. 

Orontium aquaticum, fruiting tops. 

The following may be sent in in the natural condition as col- 
lected: 

Rhizome of Dryopteris marginalis. 

Roots of Asclepias tuberosa. 

Roots of the wild chicory plant. 

Cultivated plants of the large horse sorrel (Rumewx acetosa). 

Bulbs of Calochortus, any species. 

Yucca baccata roots. 

Eurotia lanata, dried and bundled. 


53 


Atriplex patula, dried and bundled. 

Tubers of Psoralea esculenta on the plant. 

Tubers of Solanum Fendleri on the plant. 

Tubers of Solanum Jamesii on the plant. 

Tubers of Hoffmanseggia on the plant. 

Grain of wild rice in the hull. 

The same, cleaned. 

Chufas, about two pounds. 

Each specimen will be placed in the cases prominently labeled 
with the name of the donor and the same acknowledgment will 
be made in the printed Guide Book.—H. H. Russy, Hon. 
Curator 


Dr. Henry Allen Gleason has been appointed the First Assist- 
ant of the Director of the New York Botanical Garden, succeed- 
ing Dr. W. A. Murrill, who has been transferred to the new pos- 
ition of Supervisor of Public Instruction. 


Camillo Schneider, whose botanical explorations in China were 
cut short by the war, and who has been studying Salix at the 
Arnold Arboretum, recently visited the Field Museum at Chicago, 
the New York Botanical Garden, the Brooklyn Botanic Garden 
and other institutions. Mr. Schneider has been working on the 
native American willows, of which he reports the number of 
probable wild hybrids to be very great. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of TorREYA in which their papers appear, will kindly notify the 
editor when returning proof. 

Reprints should be ordered, when galley proof is returned to the editor. The 
New Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
following rates: 


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Covers: 25 for $1.00, additional covers 114 cents each. 
Plates for reprints, 50 cents each per 100. 


Committees for 1919. 


Finance Committee Program Committee 


R. A. Harper, Chairman. Mrs. E. G. Britton, Chairman. 
J. H. BARNHART, Pror. JEAN BROADHURST 
Miss C. C. HAYNES B. O. DoDGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F, J. SEAVER 
J. H. BARNHART, Chairman. Membership Committee 
R.A. HARPER J. K. SMALL, Chairman. 
N. L. Britton T. E. Hazen 
A. W. EVANS E. W. OLIVE 
M. A. Howe Local Flora Committee 
H. H. Ruspy N. L. Britton, Chairman. 
Field Committee Phanerogams: Cryptogams: 
F. W. PENNELL, Chairman. E. P, BICKNELL Mrs. E.G. Britton 
Mrs. L. M. KEELER N. L. Britton T. E. Hazen 
MICHAEL LEVINE C. C. CurtTIS M. A. Howe 
GEORGE T. HASTINGS K. K. MACKENZIE MICHAEL LEVINE 
Percy WILSON NORMAN TAYLOR W.A. MuRRILL 


F. J. SEAVER 
Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. -Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M. 
_ Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
: Gasteromycetes: G.C. Fisher Fungi-forming sclerotia: A, B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: _H. M. Richards, F. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 
Cortinarius: R. A. Harper Zygomycetes: A. F, Blakeslee 
Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H, M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurst 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


OTHER PUBLICATIONS 


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-TORREYA. 


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EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873. 


CONTENTS 
Botany in the City High Schools: F..T. HUGHES ...,..sccecseeserceeeeeeseueeeseereuereneces 57 
Changes in Teaching Biology in Our High Schools: Cyrus A, KING ooeetesseceesesaes 65 
The Relation of First Year Botany to Advanced Work: Pau B. MANN........--.-++ 72 
Reviews: 

Trelease’s Plant Materials and Winter Botany: A. GUNDERSEN..-..+s+e-.05 «+4 78 
Proceedings of) the Clubyis.. o: ox... cn cstnngustadodesvosonesivapebeqeeiecangecpecdersvane sande nowe 79 
VA RSOPLE CEG Go AEA A Clog sue, fewsta cba euraua. bp ikccbe's Ky Bae iene ueen dS tn calmnet en spts bap tee 83 
TOC WE TING re oy ven en tube ica, \ Sack as season d aus otetisoser seize rans Ae Al ie dewtie ds vccdeavansodesy yey 83 


‘PUBLISHED FOR THE CLUB 


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NORMAN TAYLOR. 


Delegate to the Council of the New York Academy of Sciences 
M. A. HOWE, Px.D. 


OFFICIAL ORGAN OF THE WiLD FLOWER: PRESERVATION 


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wVN OU Ig 


TORREYA 


Vol. Ig No. 4 
April, IgIg 


BOLANY UN.) FEE CLDY HIGH. SCHOOLS* 
By Francis T. HuGHES 


Just at present high school biology in general and high school 
botany in particular are in a very critical position. The cause I 
believe is both external and internal, but largely external. Pre- 
judice, the child of ignorance, jealousy, and even patriotism, 
strange as it may seem, are among the forces that are working 
against us from the outside. While from the inside our failure 
to recognize the changed conditions existing in our high schools, 
due to a certain complacency and false sense of security in the 
standing and permanency of our subject, has left us in a pre- 
carious situation. 

To be more specific: I shall try briefly to outline what I 
consider the external situation and the internal conditions that I 
have just enumerated, and to point out, if I may, a few remedies 
that may relieve the situation and bring botany back into its 
own in the New York City high schools. 

First as to prejudice and ignorance, which are practically the 
same thing. I heard an eminent physician say the other evening 
that the layman’s knowledge of medicine was always one genera- 
tion behind that of the specialists. And so in high school 
botany we are accused by people who really ought to know 
better, of teaching a kind of botany that was in vogue twenty 
years ago, and which we never think of teaching now. Their 
idea of botany is what they themselves studied years ago. It 
consisted of memorizing long scientific names, learning endless, 
minute classifications, and incidentally plucking a few flowers. 


* This and the next two papers were delivered at a meeting of the Club on March 
11 devoted to a conference on Botanical Education in the Secondary Schools.—ED. 
[No. 3, Vol. 19 of TorREYA, comprising pp. 37-55, was issued 14 May, 1919.] 


57 


HA, 


58 


Next as to jealousy, or rather let me call it competition among 
the various high school subjects for a permanent place in the 
curriculum. In the New York City high schools we have had 
until recently three sciences in our course of study—biology in 
the first year, chemistry or physics in the second and physics or 
chemistry in the third, with sometimes an elective in the fourth 
year. Suddenly, however, from out of the west came a gay 
young Lochinvar, known as general science and then things 
began to happen. I shall not attempt to enter into a detailed 
discussion of general science here this evening. That is a topic 
calling for a special meeting by itself. Suffice it to say that our 
friends the physicists and chemists, especially the physicists, 
at once seized upon it as the solution of many of their problems, 
and in their magnanimous and altruistic spirit worked for its 
introduction into first-year high school in place of biology. 
For years the physics and chemistry people have been worried 
over the immaturity of their pupils and the time it took them to 
learn elementary physical and chemical principles. They could 
do none of their cherished advanced work and they certainly 
were in a quandary. Therefore, when general science appeared 
over the horizon they seized upon it with avidity as a preparation 
and a preliminary subject for theirown courses. Here, said they, 
is just the thing to give the first-year pupil the proper apper- 
ceptive mass of physical facts and principles upon which we can 
later construct our real physics and chemistry. Here is our 
looked-for opportunity. Did they ever consider what this would 
do to biology? I don’t believe they ever deemed it worth 
thinking about. What I have just said about general science 
and the physical science folk may seem a trifle exaggerated. 
If, however, you wish to substantiate it, just look over the general 
science text-books that are being published and see the relative 
amount of space devoted to physics, chemistry and biology, or 
examine the topics taken up in the high schools where general 
science is now being taught. In’one high school in Brooklyn 
first-year general science is actually being taught by physics and 
chemistry teachers. That, I think, should show which way the 
wind is blowing. 


59 


Finally, in what way does patriotism affect us? As you all 
know there has been more or less Bolshevism in the schools, espe- 
cially in the high schools. The authorities have been at their 
wits ends to stamp it out and they are going to try the following 
remedy: They are going to try to conquer Bolshevism by teach- 
ing concrete practical American patriotism. They are going to 
try to show our high school pupils that their political and eco- 
nomic salvation lies in upholding the principles upon which this 
government is founded. To this no patriotic American would 
think of objecting or even disagreeing. But what is the specific 
program to be followed? In the first place economics is to be 
put into the last year of high school and no student may graduate 
without passing it. An excellent and patriotic idea, we all agree. 
Secondly community civics is to be taught in either the first or 
second year of high school with a minimum requirement of two 
periods per week for a year, and this is where we are directly 
affected. Several high schools are giving all of the community 
civics for four or five periods per week in the first term or first 
year, and biology is being forced out to make room for it. Now 
what we biologists contend is, that while community civics 
should be taught to our pupils, the place for it is in the elemen- 
tary or junior high schools and not in the regular high schools. 
I am saying this not simply because I am a biologist, but because 
I firmly believe that no other subject in the curriculum has those 
qualities which adapt it so peculiarly to first year high school 
students as does elementary biology. 

I seem to be digressing somewhat from my topic, but I feel 
that the situation is serious enough to warrant it; and unless we 
are prepared to meet it, and, meet it right now it will not be at all 
necessary to consider the kind of botany that is best for our city 
high schools. 

But to get back to my subject. What kind of botany should 
we teach in New York City high schools? In the first place we 
should begin with the pupil’s environment, the environment of 
his home, if possible, or the environment of his school or of the 
neighborhood of his home or school. This, it seems to me, is a 
fundamental principle, a sort of pedagogical commonplace, but 


60 


some teachers seem to consider it practically impossible. In its 
place they try to construct a course or series of topics which, 
though vital and necessary in the eyes of the teacher, either have 
to be forced upon their pupils or given to them camouflaged with 
all sorts of more or less interesting appendages. And what is the 
result? The pupils dislike it; they get very little good from the 
work; the subject becomes unpopular, and finally it has to fight 
for its very existence. And the whole trouble has been started 
by its friends. 

In most of our high schools where a regular course in botany 
is given, we find the following methods in vogue: Some try to 
follow the order of nature. They start with seeds and seedlings 
and working their way through roots, stems, leaves, flowers, 
fruit, wind up with a little on forestry. In other schools the 
start is with made soil composition and chemistry. In others 
the parts of the plant receive only enough attention to furnish 
the structural basis for teaching the vital processes. In other 
schools little or no time is spent upon botany as such; but most 
of it is occupied with foods and nutrition, bacteria, sanitation 
and kindred subjects. 

In contrast with the above my idea would be to include most of 
the foregoing topics, but to utilize them by linking them up with 
the most accessible and obvious botanical object the pupils meet 
with in their daily lives. Let that object be a tree or shrub or 
even a potted plant in the class room; but by all means let it be 
some tangible concrete object, some plant whole, something 
that they can see, something that they can examine and some- 
thing that they can watch grow. Let them give it a name, its 
correct botanical name. There is nothing like a name to give a 
thing individuality. Let them consider it a member of a class, 
—a non-resident member if need be—but a member just the 
same. 

If the pupils are fortunate enough to be raising a war garden, 
then let that be the center or nucleus upon which their botanical 
work is based. Children of the first-year high school age are 
very practical and matter-of-fact in many ways, and while it is 
sometimes a hard job to get them interested in plants in general, 


61 


it is the easiest thing in the world to get them interested in some 
one particular plant. It is like their instinct for keeping pets. — 
The average boy is not so much interested in dogs in general,— 
in the way a grown-up lover of animals is apt to be. What he 
cares particularly about is his dog Jack and in his mind all the 
other dogs in the neighborhood are just plain dogs. 

If the object selected for study be some particular tree or 
shrub, the next thing to do would be to get a picture of it and 
hang it up in the classroom. If one of my pupils had a camera 
I would have him take a photograph of it, or in lieu of that I 
would have one of the pupils make a large drawing of it. At any 
rate if I could not get the plant into the classroom, I would have 
its picture there. 

Some may raise the objection: What concrete botanical object 
can be found in the environment of a lower East Side high school 
boy? What trees, for example? Let us see. A great many of 
such boys go to either DeWitt Clinton or Commerce or Stuy- 
vesant. None of them have trees or shrubs about their homes 
and so far as I can recall there are none either near or on their 
school grounds? But do you realize that DeWitt Clinton, situ- 
ated as it is in one of the most congested and botanically unde- 
sirable sections of the city, is only two blocks from Central Park 
and many of the boys pass the park on their way home. Com- 
merce also is but a short distance from the park. Every other 
high school that I can think of either has trees around it or has 
one or more small parks in its neighborhood. If the high school 
is in the suburbs or outskirts I would select a tree or shrub from 
in front of a pupil’s home. 

, But why begin with a tree? For one reason because it is large. 
There is something about size or bigness that seems to appeal to 
the average high school pupil. It is his idea of greatness or value. 
Did you ever notice the smile or look of contempt that comes 
over a boy’s face the first time you hand him a bean to examine? 
To him a bean is something to eat or to play with, but not to 
study. It may be all right for elementary school pupils to raise 
seeds in a cigar box, but not for him. 

Another reason for selecting the tree is that it is likewise the 


62 


botanical object most familiar to the pupil’s parents and there- 
fore the most likely to maintain their respect. On the other 
hand a seed suggests the farm and the average city parent, thinks, 
if he thinks about it at all, that farm topics do not belong in a 
city high school. I may seem to be emphasizing too much the 
parent’s opinion of things, but the strongest ally of any subject 
is the sympathy and coéperation of the parents. JI am not saying 
this in a spirit of opportunism. But if we believe our subject is 
worth while and good for the pupils we should do everything 
possible to disarm criticism from the home and by a judicious 
amount of tact and resourcefulness lead both parents and school 
officials around to our way of thinking. There is an old saying 
and a true one: ‘‘You cannot catch flies with vinegar.” So 
do not begin your subject with an altogether strange or uninter- 
esting topic. 

In connection with this let me repeat a story I heard a short 
time ago about a parent’s objection to botany. This parent had 
a daughter studying botany in one of our suburban high schools. 
One day he asked her the name of the tree in front of his house. 
The zirl did not happen to know the name and the father began 
to wonder what kind of botany his daughter was studying. 
Thereupon he called upon his daughter’s teacher and politely 
told him that botany should be thrown out of the schools and 
something more useful put in its place, since his daughter could 
not tell one tree from another. In answer to this complaint the 
teacher said: ‘‘My dear Sir, naming and identifying trees is but 
a small and insignificant part of botany. What we teach is the 
more fundamental life processes; then later on if we have the 
time we take up classification.’’ Was that teacher right? 
Substantially and in the matter of content, yes. But in the 
manner of approaching his subject or parent as the case may be, . 
I think that he was wrong. The parent’s criticism may have 
been captious and insincere, but he had some grounds for it just 
the same. 

Now as to the way in which we should go about the detailed 
treatment of the tree or shrub. If I began with the fall term I 
would start with the leaves and their structure. After that I 


63 


would take up respiration, transpiration, photosynthesis, etc. 
But how would I get enough leaves from a city tree to supply 
all of my classes, especially when there is a park ordinance against 
picking leaves? I would not try to get them from the city tree. 
I would get them in the country during vacation time or on 
Saturday or Sunday. That, I do not think, is too much to do 
for one’s subject. 

How are we to teach the vital processes? Are we to rig up a 
set of apparatus on one of the park trees for the wonder and 
admiration of the passing throng? Not at all. I would demon- 
strate the different functions in the classroom with the same 
materials and apparatus that I always use, but I would refer 
everything to our chief object of study and constantly remind 
the class that they were observing not only what trees in general 
are doing, but also what one tree in particular was doing in order 
to keep itself alive. 

What about the flowers and fruit of a city tree? That seems 
an almost unsurmountable obstacle but it is not. Its very 
difficulty gives zest to its solution. If the average city person 
knew that oaks and elms had flowers and fruit he would pay 
little attention to it. But the element of surprise that strikes 
him upon first being made aware of the fact first excites 
curiosity, then arouses interest and finally holds his attention. 
It is not the entirely new that arrests our attention, nor the 
completely familiar; it is rather the one in connection with the 
other. It is the old in the midst of the new, as when a traveler 
hears his own language in a foreign country—or the novel in 
the midst of the customary—as when we hear a strange tongue 
that attracts attention. 

But to get back to the flowers: I would not attempt to teach 
them at all directly. I would have a chart or drawing of the 
flowers of that particular tree or shrub. But I would give a 
complete set of lessons on the most available flower, I could get 
at that time of the year, but as with the leaves I would constantly 
refer them to our main object, the tree. 


spoken in our own country 


The fruit I would treat in the same way, using the tree’s own 
fruit if available; if not, then some common fruit in its stead. 


64 


The next topic is the stem. To teach this we should have cross 
and longitudinal sections of the same kind of wood. Branches 
of almost any kind can be secured from the Park Department; 
their wagons will deliver them to the schools and the boys will 
be only too glad to saw them up into sections and even varnish 
them for you. This I have had done several times. All that it 
requires is a letter to the Park Superintendent. As for the other 
parts of the tree I would not spend much time on them, but I 
would put most of the emphasis on the leaves, flowers and fruit; 
and would treat the rest only enough (in a general city course) 
to show their functions and their relations to the food making 
and reproductive organs. 

Having thus taken some common shrub or tree as our type 
form and taught the structure, functions and adaptations of the 
principal parts, I would then take up any other botanical topic 
best adapted to the needs and environment of my pupils. With 
one set of pupils I should emphasize the economic importance of 
plant products and by-products as food; with another group, 
especially where there was a manual training department I 
would spend much time on woods, their kinds, uses, etc.; and 
so on selecting my topics according to the needs of the various 
classes. 

My idea in advocating the study of some one particular plant 
as outlined above is this: Heretofore we have been studying 
seeds with the bean and corn as types, roots with the carrot and 
parsnip as types, and stems with the oak sections and horse- 
chestnut twigs, but somehow or other the pupils never linked 
them together. To them the bean did one thing, the carrot 
another, the horsechestnut twig a third and so on. They did 
not connect them all with the plant as a whole. On the other 
hand I think, that if we take one complete object, treat it as a 
whole and in detail, we will secure greater concentration and 
develop more fully the fundamental mental processes of analysis 
and synthesis. We can show the relation of the whole to its 
parts and the parts to the whole. 

Paralleling all of this work and in close connection with it, as 
one of its most valuable features, I would use to the very fullest 


65 


extent possible our botanic gardens and museums. I would not 
look upon them as a mere adjunct to our work or as factors in a 
method of teaching, but I would connect them as an integral 
part of the subject and-in one sense the most important part. 
If the training and botanical knowledge that we give to our 
pupils is going to amount to anything it must not stop at the end 
of the first year course in elementary botany. How then are we 
going to continue it, especially with those pupils who cannot go 
to college? The answer is, teach them how to use the gardens 
and the parks. Teach them so that in later years and even 
during the rest of their high school course, they may find in 
them a place for recreation and a source of inspiration, a means 
of avocation, and in some cases, let us hope, a field for serious 
study. What the public libraries are to the English and history 
departments, the gardens, parks and museums should be to the 
biology department. 

In conclusion let me say that though the present outlook is 
’ none too bright, and we may have to fight for the very existence 
of our subject, the future is not hopeless. If we believe in our 
subject let us vitalize it. Let it meet the needs, solve the prob- 
lems and arouse the interests of our pupils. If we do this, if we 
vitalize it properly, botany will compel its own recognition. 


Boys HIGH SCHOOL, 
BROOKLYN, N. Y. 


CHANGES IN “DEACHING “BIOLOGY “IN; OUR Hie 
SCHOOLS 


By Cyrus A. KING 


To graduate from a city high school, a pupil is required to pass 
and receive credit for 17 units of work. Of these units, eight 
are required of all pupils. Three are in English, three in history 
and civics and two are given for work in drawing and physical 
training. The other nine units are selected from the following 
groups: Three from a foreign language group, two from another 
language group, two from the mathematics or science group, 
and the remaining two from any group. 


66 


This seems an admirable arrangement, and at first glance, one 
might think it offered a wide range of selection to suit the indi- 
vidual wishes of different students. However, when we con- 
sider the traditions of the high schools, and the still more rigid 
traditions of our eastern colleges, we find that the sciences are 
practically cut off from our best class of pupils, the ones who 
intend to go to our higher institutions, and who, in consequence, 
are ultimately to be our most influential citizens. 

I propose to illustrate this by selecting three typical examples. 
Let us suppose that a boy wishes to prepare for an engineering 
school. In addition to his eight credits, which are required, he 
selects a language and carries it three years; this leaves s7x units. 
Our best engineering schools require four years of preparatory 
work in mathematics; this leaves two units. These are usually 
taken in physics and chemistry because they are often required. 
This boy has no chance to select the biological sciences, unless he 
takes them as extra subjects. 

Let us now take the case of a girl who wishes to enter one of 
the better girls’ colleges, for example, Mt. Holyoke, Smith, 
Vassar or Wellesley. In addition to the eight required units, 
she must have four units in Latin, at least fwo in a second lan- 
guage, and two and a half in mathematics. This leaves one half 
point for science work. 

For the third illustration, we will select a pupil who does not 
intend to go to college. The traditions of most of the academic 
schools will cause him to elect a modern language, which he will 
carry for three years; he will also take at least two years of mathe- 
matics; this leaves four units to be selected from a second lan- 
guage, from courses in stenography and typewriting, and from 
the different sciences. Let us suppose that he selects two sciences 
the question 1s shall one of them be a general course or a course 1n 
biology. 

The biology courses that are now offered in our city high 
schools are, relatively speaking, new. They have no inheritance 
and no traditions. Unlike Greek, Latin and mathematics, 
they have not occupied for centuries an important place in our 
educational institutions. They are so new that we have scarcely 


67 


had time to stabilize them. However, there has never been 
such an age as the present. Days count almost as years of 
certain earlier periods. Under such conditions, a modern subject 
is rapidly adapted to our educational needs. Furthermore, 
biology certainly has the merit of having had no opportunity to 
become fossilized. 

Our elementary course in biology was born about 1900, was 
revised thoroughly in 1905, again in 1910, and a new revision has 
just come from the press. The advanced course in biology was 
approved three or four years ago. It is now undergoing a 
revision. 

During this interval of twenty years, the aims of the course 
have broadened and the work became more definite. And now at 
the end of this time, when we have the best courses that we have 
ever had, when we have a corps of highly trained efficient teachers, 
and know that ours is one of the most valuable subjects in the 
whole curiculum, it is actually being forced out of the schools for 
a conglomeration of every thing in kingdom come which for lack 
of a better name is called general science. The New York City 
schools are now teaching general science without a syllabus and 
without specially trained teachers. 

I have looked over about a dozen text-books in general science, 
some good, some fair, and some poor, and have the honest con- 
viction that the subject, at the present time, is not well organized. 

True to their name, our biology courses center about life and 
living things. Their aim 1s to teach the fundamental principles 
of life and it is impossible to develop these principles in the limited 
time given to the subject in a general science course. To accomplish 
this it is necessary to study a number of forms that are widely 
different. This is why we have put into our courses a consider- 
able amount of plant study, a somewhat less amount of animal 
study, and, finally, a study of man with an application of these 
principles to him. We believe that a pupil who has proved 
that respiration takes place in germinating seeds, that it takes 
place in higher plants, that it is necessary in the life of the para- 
mecium, who understands how the insects, the fish and the frog 
are adapted for breathing, and who knows something of the organs 


68 


of respiration in man and their adaptations, sees a deeper meaning 
in respiration as a vital process. The same thing applies to the 
great facts of sex reproduction, inheritance, and eugenics. Our 
course requires that we work with living things that throw light 
on the fundamental problems of life. 

At the risk of being called old fashioned, I do not hesitate to 
say that the foregoing kind of work is the most important that 
can be offered in any course in biology. And what are the reasons 
for not having such a course in every high school? What kind 
of an education is it that fails to recognize the value of the study 
of man as a living organism. Mentally and physically, he is the 
center of all education and he is unified with and bound to these 
lower organisms by the laws of life. Furthermore, if an addi- 
tional argument were needed, we know that the study of plants 
and animals trains him in observation, develops his judgment, give 
him the method to reason logically, and finally furnishes him with 
important information about himself. It also opens up a new 
living world that he will appreciate all his life. 

Recently a father, who by the way is a strong advocate of 
general science, said to me: “Your biology work is not making 
good.” I asked him why he thought so and he said that his 
daughter had taken the course for a year and did not know the 
names of the trees on the block where they live. This, in his 
opinion was a serious criticism. My answer to this is that our 
course requires that we place the emphasis chiefly on important 
biological problems and that this leaves little time for such 
superficial work as learning names, even though this is desirable. 
However, before passing in the course, that daughter had to 
know the general structure of a root, the way it gets water from 
the soil, and she had seen this illustrated in the laboratory. 
She had to know the course of the water through the root, stem, 
and leaves; and she had seen experimental proof of this. She 
learned by experiment how plants give off water and something 
of how food is manufactured. She knew, too, that this tree took 
in and gave off certain gases and the reason for this exchange. 
This incident illustrates the type of criticism that we are re- 
ceiving. In the main, it comes from persons who have no con- 


69 


ception of the value of our work, who are more or less antago- 
nistic to it, or who have their ears on the ground listening for 
something new. 

A second aim of the course, is to emphasize the relation of 
biology to human welfare. This brings out the commercial 
importance of plants and animals and our dependence upon 
them; especially upon plants. It is a revelation to our city 
boys and girls to find that the aunual value of our corn crop is 
greater than any liberty loan except the fourth, and to learn that our 
wheat and oats crop in 1917 were about two billion dollars each. 
Only after they realize the tremendous importance of our crops, 
do they appreciate the damage done by plant diseases and insect 
pests. One writer, for example, estimates that the hessian fly 
and the wheat rust each destroy one tenth of the crop. While 
this may be an exaggeration, it nevertheless suggests the im- 
portance of biology to our daily life. It is an introduction to 
the study of agriculture in its various phases, to pharmacy, to 
dentistry, and to medicine, and it also interests them in the laws 
of inheritance and in plant and animal breeding. 

The study of bacteria gives a second important relation to 
human welfare. The names and structure of bacteria are of 
little importance to our pupils. But it is important that they 
know the conditions under which bacteria thrive well and the 
conditions that cause their death. Pupils should know how 
abundant they are, and the common ways of distributing them. 
These lessons are necessary to emphasize the third point in my 
paper and that is that our biology courses are an excellent train- 
ing for citizenship. 

Twelve years ago, when the American association met here in 
New York, one of the foremost biologists in this city read a paper 
in which he emphasized the importance of biology in the develop- 
ment of citizenship. While I will confess to you that I had not, 
up to that time, thought of our courses as especially valuable in 
this respect, I have never since lost sight of its possibilities. 

Heretofore, I have been quite willing to let the philosophers 
and the theorists discuss the subject matter best adapted for the 
development of citizenship. The subject belongs largely in the 


70 


field of the general and the abstract where the philosopher 
revels. 

It is my opinion that the biological sciences can supply excellent 
material for the development of citizenship and I propose to 
offer some definite suggestions that show what we can contribute 
to this work. A citizen is a person who is born in the United 
States or who has been naturalized here, who owes allegiance to 
his country, his state, and his city, and who is entitled to their 
protection. The opposite to a citizen is an alien. Our war has 
emphasized the importance of eliminating the aliens and edu- 
cating the citizens. 

Mention has been made that we teach the importance of 
bacteria in relation to human welfare. Our pupils know the 
danger of infection from milk, why unsanitary stables are a 
menace and why the men working in the stables should not come 
from homes where there are communicable diseases. They 
know that milk should be subjected to a low temperature at once, 
why it should be Pasteurized, and the care it should have while 
on the way to the city. This is equally true of meats and vege- 
tables. Our pupils know the danger from inattention to the 
water supply. They appreciate the importance of clean streets. 
Their knowledge of epidemic diseases will cause them to favor 
and insist upon an efficient board of health. They have sane 
reasons for supporting regulations relating to quarantine vacci- 
nation and disinfection. They have a more intelligent interest 
in the care of our parks and the trees of the city. Such educa- 
tional institutions as the botanical gardens and the American 
museums will get their hearty support for they appreciate what 
these institutions stand for. They have a more intelligent 
interest in, and a greater loyalty for their city. They are better 
equipped to assume the duties of citizenship. 

It is possible that the advocates of general science, who by the 
way, are chiefly teachers of physics and chemistry, will tell you 
that their course does all thisand’a great deal more. My answer 
is that it would be better to have two years to do the work out- 
lined in biology. When they give the biology work a minor 
place in a year’s course, they simply mutilate it. Pupils grasp 


71 


the great questions of life only after having studied them in a 
reasonably wide range of individuals. In comparing the value of 
the two courses, do not lose sight of the fact that our work is a 
matter of record and we are perfectly willing to be fairly judged 
by what we have done and are doing. Theirs is all theory and 
argument. I have never heard a general science advocate give a 
concise, constructive argument for its substitution for biology. 
They will tell you that it has made good in the West, and that it 
is spreading everywhere. There are several reasons why I am 
not much impressed with that argument. First, the West is a 
long way off and it is not possible to get definite facts as to how 
successful their work is. Second, the universities of the Middle 
West are less exacting in their conditions for admission. This 
leaves plenty of time for three or four years in science courses. 
Such conditions will offset the handicap of one inferior course. 
In the third place, I have personally admitted to our courses 
pupils who have been trained in general science in schools 
at Minneapolis, Chicago, Washington, D. C., Massachusetts, 
Connecticut, Pennsylvania and New Jersey. This list includes 
one pupil who was taught by the author of one of the well-known 
books in general science. In every instance, I examined the 
laboratory note book, in case the pupil made one, and the results 
make me more emphatic in saying that general science, as taught 
at the present time, is not well organized. 

And now, in conclusion, to revert to the title of my paper, the 
changes that I would suggest are not so much the content of the 
course as the question of emphasis. I would urge, first, more 
time on the fundamental processes of living things. This is the 
most important part of the work and unless we get our pupils to 
understand them, by teaching them over and over again, we will 
lower our course until ‘t is on a level with general science. Second, 
wherever possible, I would teach these principles by means of 
forms that have an important relation to human welfare. Third, 
I would emphasize facts in our course that train for citizenship. 


Erasmus Hatt HIGH SCHOOL, 
BROOKLYN, N. Y. 


72 


tHe RELATION OF Piksi), YEARY BORANY SOR ae 
VANCED) WORK. WIDTH REPERENCES) iO} Clik 
DAUNPAP EEG MONS AND) BYEPRODUGHS 


By Pau. B. Mann 


The present fluid and even kaleidoscopic status of elementary 
biology in New York City high schools, reminds me forcibly of a 
bit of doggerel which appeared years ago in Harper’s Magazine. 
A colored man had been exercising his mule in the plantation 
garden, but an altercation arose between them, resulting in the 
sudden juxtaposition of Rastus’ head with the distal extremity 
of one of the mule’s hind legs. Rastus went to sleep. Later | 
consciousness began to dawn and he sat up and soliloquized in a 
mournful way, beginning: 

“Ts dis yuh me, or not me, 
Or hab de Debil got me?” 

We will all grant that the world needs men and women of 
scientific imagination and better viewpoints. ‘Where there is 
no vision, the people perish.’’ The march of progress can be 
checked by observing the scrap heaps along its highway. But 
one might well be perplexed when one finds any inconoclastic 
authority throwing bodily to the discard-pile, a vehicle which is 
having one of the most conspicuous careers in advancing human 
achievement and aspiration. 

I have not only hope, I have faith that even arbitrary action 
can not finally overthrow biology nor displace it permanently 
from its position as a science of fundamental values for adoles- 
cents, as well as adults. 

The most discouraging phase of the present situation in the 
New York City high schools, it seems to me, is the possibility of 
a hasty, unpedagogical ipse dixit, unsupported by judicial and 
scientific investigations. 

Dr. Josephine Baker, in a recent lecture, spoke of the tre- 
mendous need of conserving the Belgian children now, from 
rickets and tuberculosis, if Belgium is to be! We know, but 
sometimes forget, how truly the structure of the nation of to- 


morrow is being builded today. But how can the nation have 
well rounded and stalwart thinkers in its tomorrow if the edu- 
cators are given the children (the raw material), and then imme- 
diately handicapped not only as to tools but as to methods of 
development? The men and women who were pupils in such a 
system, will some day declare the bitterness of such injustice. 

Of the many contributions which elementary botany and 
biology make for advanced courses in the school and for later life, 
I wish to refer briefly to five. 

In the first place, the subject of human reproduction is 
intimately associated with the highest hopes of humanity, and 
yet is connected with some of the most sordid problems of the 
race. The very insistence of the sex problem compels a genuine 
answer from the schools. That answer must be sound, thorough 
and immediate. Let me quote a line from a letter just received 
froma Y. M.C. A. workerin France. ‘‘It is our former American 
interpretation of those two terms [morale and morality} that 
disturbs me in trying to consider what America will feel toward 
and do for her men who are soon to return to her. Is she going 
to continue to say that there is no sex problem in life, or is she 
going to face it squarely and try to solve it?”’ Those who have 
studied the problem of. presenting sex matters to children and 
have taught biology, know that to avoid the pitfalls there must 
be a natural. and unforced approach. There is absolutely no 
substitute for the normal, logical procedure of our elementary 
biology courses, dealing first with fertilization in the flowering 
plants, then in a typical animal like the fish or the frog. Neither 
of these topics when presented is tied up with sex-hygiene, there 
is no self-consciousness, and there is built up a natural foundation 
for all later applications, whether of sex-hygiene of one sort or 
another, or the justifiable expectations of the instructor in 
advanced botany or zodlogy. 

In the second place, the stress given to hygiene, now con- 
tinued throughout the entire high school course, might lead some 
to a presumption that elementary biology could fairly be dis- 
pensed with, in view of the probable(?) duplication of subject 
matter and treatment. However, the situation is far from being 


74 


so palpable. There need be little duplication. In addition, 
since the hygiene is largely deductive, it presupposes thorough 
grounding in biologic principles and bases. Military autocracy 
can be exemplified by the lines “Theirs not to reason why,”’ 
but the full codperation of the average hygiene student, and 
indeed every adult as well, in health endeavors as in other lines 
of action, is gained not only by knowing that “‘there’s a reason,” 
but knowing what that reason is. First year biology supplies 
abundant reasons. There is neither time, with only one hygiene 
period a week, at the most, nor is there continuity enough 
possible, to teach the content of a full year of biology by means 
of such a hygiene subterfuge. Daily contact with the experi- 
mental evidence of the laboratory is requisite for mental digestion 
and assimilation of principles, and to develop the scientific view- 
point. Last term, for instance, one of my hygiene classes had 
to be excused from one week’s recitation on account of a holiday, 
and the next week did not recite for another reason. That 
meant that they went three weeks without a single recitation! 

Nor is there much encouragement for the man who feels on 
the other hand that general science presents enough biology to 
be a worthy substitute. I shall not enter into the relative merits 
of these two subjects. Each hasits place. However, the amount 
of biology presented in a year of general science is too frequently 
insignificant. 

In the third place, have we any moral right to deprive 
students of the cultural values which are unquestioned by- 
products of elementary biology? Whatever philosophy of life 
each student comes eventually to formulate, early or later, will 
hinge on living things and their relation to metaphysical ques- 
tions. The drama of life is unbalanced and ill-proportioned if 
viewed through anthropocentric lenses. Literature is full of 
references to nature. Shall we send our pupils out into the 
world, into nature itself, refusing them the key to the inter- 
pretations of biologic phenomena? For each student, is due at 
least the opportunity of an esthetic appreciation of the wonder of 
life and of the utility and beauty of its types, whether diatom or 
humming bird, scaled mosaic from a butterfly’s wing or the 


75 


perfect spiral of the chambered nautilus. In this connection, 
Professor Curtis writes as follows:* ‘‘The writer remembers how’ 
when a student he was taken by the ‘ Mosquito-Malaria Theory,’ 
as it was then called; and at a later date the esthetic appreciation 
with which he contemplated the apparent explanation of Men- 
delian segregation and of the determination of sex in terms of 
the behavior of chromosomes. In spite of uncertainties and 
the need for further investigation, one felt himself gazing at a 
picture near enough completion to show what it might become 
—a sequence so wonderfully ordered as to call forth an esthetic 
fervor.”’ 

Then again, how without studying elementary botany, can 
we count on an intelligent citizenry, a citizenry personally 
interested in forest conservation, individual, municipal, national 
and inter-national nutrition, including problems of soil fertility, 
crop production, plant diseases and insect pests, improved 
methods of transportation and preservation of foods, selection 
and utilization of proper woods, and a host of related problems, 
such as the substitution of kelp as a potash source, the ascer- 
taining of new plants yielding rubber, etc., not to speak of applied 
bacteriology and commercial products. The balance of the 
year of biology includes the bases for the conservation of fishes, 
birds and other wild life and the economic relations of hundreds 
of animal types, from parasites to makers of silk, producers of 
fur, buttons, oil and so forth, together with an intelligent appre- 
ciation of rational living for humans, themselves. 

The significance of botanical training has been lately tested 
in a large way. We know how thousands of boys and girls 
sprang with avidity to the gardens and farms of the nation, 
during the past two years, and applied there the laboratory 
methods of their botany and biology courses. Furthermore, 
they were trained and ready to interpret the dietetic problems 
for the rest of the family and thus they kept up the family morale 
by doing their full share in emphasizing all phases of Hooverizing. 

Then there are legislative opportunities. For instance, to 
refer to only one example among many, last year we needed 


* Science, June 14, 1918. 


76 


intelligent legislators, with biological training to pass the Week’s 
Bill, prohibiting the uninspected importation of nursery stock 
into the United States, and thereby preventing the introduction 
of plant diseases and obnoxious insects. New bills of biological 
import will continue to be introduced at Washington and in the 
state legislatures and there will be even more call for their in- 
telligent consideration. Shall we turn back the hands of the 
clock and parallel the situation in Pennsylvania in 1885, when 
an unbiologic legislature spent in hawk bounties, directly and 
indirectly, nearly $4,000,000 to save a paltry $1,875 worth of 
poultry? 

Finally every one recognizes the growing emphasis that the 
latest decade has given scientific achievement and progress. This 
appreciation has been reflected in many ways. From a botanical 
standpoint alone, professional activities have had to grow by 
leaps and bounds, in order to keep pace with the demands of 
the hour. Forestry has expanded into a ranking science, the 
Bureau of Plant Industry has had to continuously increase its 
staff, plant pathologists are called upon daily to save thousands 
of dollars’ worth of plants by prophylaxis or treatment, phar- 
maceutical stations have been inaugurated, new plants are being 
originated by scientific breeding, the Office of Foreign Seed and 
Plant Introduction have brought to us valuable exotics and 
have also raised the bars of quarantine against ‘“‘undesirable”’ 
foreign? plants, physiological chemists and bio-chemists are 
everywhere at work on problems of soil fertility, fabric utiliza- 
tion, by-products of plant origin, and the like. Yet I have 
merely suggested some of the types of botanical activity, without 
reference to even a complete resumé. | 

Some of us may not realize the extent to which the national 
government and the states have fostered the development of the 
agencies calculated to answer the agricultural demands of this 
country. 

In one of the weekly news letters of last summer, Secretary 
Houston, of the Department of Agriculture, pointed out that 
there are 67 agricultural land grant colleges and experiment 
stations in the United States, with an equipment of $195,000,000, 


77 


a teaching staff of 5,900 and a resident student body of over 
75,000. 
On May 15, 1862, Abraham Lincoln signed the act, creating 


the great Department of Agriculture. In the 57 years inter- 
vening, there has never been a time when the country at large 
has been so appreciative, as at present, of the value of this 
department, nor so cheerfully contemplates the expenditure of 
approximately $65,000,000 for its supporting annual budget, to 
maintain its staff of more than 20,000 people. 

Furthermore, on May 8, 1919, there was enacted the Ex- 
tension Act, which provides that all extension and demonstration 
work shall be codrdinated and carried on coédperatively by the 
state colleges of agriculture and the Federal Department of 
Agriculture. After 1922, there will be available approximately 
$8,700,000 for a the support of this Act. The field work in each 
state is supervised by a director of extension and is done by (1) 
men county agents, (2) women county agents, (3) boys’ and 
girls’ clubs, (4) corps of specialists.* 


If, as Professor Amesj and many others contend, the war was 
really won by science, either pure or applied, then there is an 
everlasting debt which humanity owes to the men of science: 
the physicians, engineers, sanitarians, meteorologists, geologists, 
botanists, zodlogists, physicists and chemists. Their service 
sustained the world at the time of its greatest need. What I 
want to emphasize is that the careers of these men and women 
were made possible to them and to the country by their courses 
in the high school pertod of their education, when they were 
self-discovered and when they unquestionably got the trend for 
their particular vocation. 

Shall we not continue to need trained botanists, not to speak 
of other biologists? Let us keep wide open the door marked 
“Biologic Science” and let all the students of our high schools 
have an unobstructed view of whatever perspectives and vistas 
they can see. 

This then is what I have attempted to present: 


* Weekly News Letter of Department of Agriculture. 
T Science, Oct. 25, 1918. 


78 


First, the imperative need of a natural biologic approach for 
the presentation of rational sex hygiene. 

Second, the weakness of the attempt to teach hygiene without 
previous biology foundation, also the impossibility of successfully 
substituting either hygiene or general science for biology. 

Third, the moral demand upon us to supply through biology 
courses, the working material for individual culture and philos- 
ophy. 

Fourth, the necessity of popular biologic education to insure 
worthy legislation. 

Fifth, the loss to the country and to the individual concerned, 
of not discovering those whose talents and genius lie in the line 
of biologic heritage. 


EVANDER CHILDS HIGH SCHOOL, 
NEw YorK CIty. 


REVIEWS 


Trelease’s Plant Materials and Winter Botany* 


These two valuable pocket volumes contain a great amount of 
clear and condensed information about trees and shrubs. The 
former takes up 247 genera, 782 species, 1,150 forms. It is 
intended to enable any careful observer to learn the generic and 
usually the specific name of any tree, shrub or woody climber, 
likely to be found in cultivation in the eastern United States, 
except the extreme south. The concise key to genera, separate 
for trees, shrubs, undershrubs and woody climbers, emphasizes 
vegetative characters. In the main part of the work the genera 
are more fully described and keys lead to the species and forms. 
In a few genera such as Crataegus, Cotoneaster, Philadelphus 
and Rosa, only the most easily recognized species have been 
admitted. Trees and shrubs of the orchard are traced to their 
species. 

The larger ‘‘ Winter Botany”’ much surpasses any existing work 
as a practical means of identifying cultivated trees and shrubs in 

* Trelease, William. Plant Materials for Decorative Gardening. The Woody 
Plants. Pp. 204. i917. Price, $1.00. 


Winter Botany. A companion volume to the above. Pp. xi +394.  Illus- 
trated. 1918. Price, $2.50. Both published by the author, Urbana, IIl. 


79 


winter. The introductory key to genera by winter characters 
covering thirty pages is very interesting, the first division being 
according to whorled, opposite or alternate arrangement of leaves. 
The genera and species are then taken up with. It contains 
numerous excellent line drawings especially of leaf-scars and 
buds. There are many references to other works. The nomen- 
clature follows Bailey’s Standard Cyclopedia of Horticulture, 
synonyms being given where manuals differ. 

The implied future publication of a similar work for herbaceous 


plants will be awaited with interest. 
A. GUNDERSEN. 


PROCEEDINGS OF THE CLUB 
JANUARY 14, I919 


The annual meeting was held in the lecture room of the De- 
partment of Botany at Columbia University. President Rich- 
ards called the meeting to order at 8:15 P.M. There were 20 
persons present. The minutes of Dec. Io, 1918, were read and 
approved. 

The nomination of Dr. George E. Osterhout, Windsor, Col., 
Mr. S. A. Lurvey, South West Harbor, Me., and Miss Anna G, 
Runge, 577 Ninth Av., Astoria, N. Y., followed. 

Mr. Percy Wilson read the report of the Field Committee 
which was accepted. The report of the Program Committee, 
Mrs. E. G. Britton, chairman, was read by Dr. Seaver. A sug- 
gestion that in the future some of the Tuesday meetings should 
be held at Columbia University was discussed by Prof. Harper, 
Prof. Hazen, Dr. Barnhart and Mr. Taylor. 

Dr. M. A. Howe reported briefly for the Committee on the 
Fiftieth Anniversary Celebration. A statement of the receipts 
and expenditures, as follows, was read: 


SEMI-CENTENNIAL FUND 


Receipts 
angie reece vediatl. BOUT + che Coe ee Ba eee Ae Le ee $1,580.50 
PANTONE ECELV EC All: EO}LO crate cle aie ae een inne ere giover ha rtis eae Siehale we als 548.00 


$2,128.50 


80 


Disbursements 
Paid the New Era Co. Printing Memoir, Etc................ $1,373-67 
FETS AN ATT ORI te cok eae aly fel Seculscun tea rece cue sie BMA Bt o-oo ae Deer oto hai cls 153.87 
(CATA ECSous [ay Sia INST OP ONE) cca ORR E Ouch aes eee old) Geehche io oneL Binet encia.o 2.00 
EV TAVIELO PES ee ere icHees case ales eile eS Ie eee EI Se nee ears ene epee 3.60 


Editorial Expense 


BAAN C ES, ccc test te ea) ok Leek yay SBOE ase ea am Pelt ee REST Meet nee) Tae a sh et 501.51 


The treasurer reported on the estimated cost of reprinting 
Vol. 15, No. 9, of the Bulletin. It was voted to have this number 
reprinted at a cost not to exceed $40 for 100 copies. The secre- 
tary was directed to call the editor’s attention to the announce- 
ment on the cover of the Bulletin, relating to holding the Tuesday 
evening meetings of the Club at the American Museum or Colum- 
bia University. 

The resignations of Miss Henrietta Lisk, Dr. L. O. Kunkel 
and Mr. James G. Scott were read and accepted. 

Miss Runge, Mr. Lurvey and Dr. Osterhout were then elected. 

Reports of officers. 

The secretary read a report which was accepted. 

The treasurer’s report was read and referred to an Auditing 
Committee consisting of Mr. Norman Taylor and Dr. Francis 


Pennell. A statement of the receipts and expenditures of the 
Club follows: 


RECEIPTS 

Balances Conmub xchange Bank sjamilanys 7s) LOUGre acaricides ener ienenene $1,735.27 
IMGemalorenS” GINES> 5d ooo ade Roce ee eOAs Bonen EDS Pacers BA! 8 $ 970.00 
Segzunovbaver sonveronloveyasy” CESS ologaccauoceonopden000dan G0 cdOd000 90.00 
BULLE Girne peers ene ee eta i alles de be ois, heal se) ayeceye hea Preteen nectar oniet's 1,043.22 
ROR RE MAMET AER CRIT eo Leica Ge Hit at Beith a pee 183.98 
ARORRE VA OIt pure asic te retel he ro sicaits raueeceek sgsiceisiee) <tleusccitabiate fox’ Porelgayie late nenec 100.00 
INAV ET CISTI OPE Ine UNMET Cometic denis A ccerioeaivaara nice easter ekconirele ai chelaenere 72.00 
IVES TITOIRS hy ceeee Ceo ence aresoehs Mares reo el clafade ianminate Wren enoe estat 641.01 
LTV EXACAT SANs ee eM a its eas ie Recs iomce ht eac seks Muerte, eucties chee aie hele es 170.28 
SUMANICS a oh cues sustens iouevalt = toyed: susiey Meo shania’ shied bays Vee eet Race Meee 0 aS I.05 
Semii=CentenmnialMerticdeecreweroucueteceperctaletorelicuc coeheds: eirchsyie tatitcre terete) odabe 548.00 
Interest, Underwood Fund: P 

EUEOMI MBA e eee oie even aie archers seeetseced Fiat vey, eoleus sels, oun erate renee $50.00 

ir OTB OT eters ce cmeucis otek seokepoliay dats witecays. o eueneyiel otic wane as) oweneptelte I4.90 64.90 


o 


$3,884.44 $3,884.44 
$5,619.71 


81 


DISBURSEMENTS 


RIPE Lect hy hoe Sainv arash ays coe eter ANe a aIR PEA cw Wate stasdieretes ecard 75.290 * 
DORSET UA oa 8 aye Mae csc Sa hen’ sts APR DLs en cAaP eR sac si cea eG MESS BAM eas A ein 625.41 
MRP RLRESATICAS alate: Gls teh ae cious rah OIG he aries Lig ign ree Gee ee tn 307.29 
PEEHELOUMOXPODAES Ce thts Se Lay ois es Maes abre ERY Cee AU 440.62 
aM UTESEL AGERE aires eilsvers, sint akc, pte eal Save SMO Oe ah eT eee eaters Le 3.20 
BOMEIO IES core sore hy c Shcy ial Mate a Er anion Ri ances leer eee Ria ees 1,512.07 


$5,362.78 $5,362.78 


Poameen Conn XCUAN Pe yan Kin ei aiate Sudiics wttice boas aL ahtale ds eeideleie. clears 250.63 


Funds on deposit Union Square Bank...................:. 


Wnion square Savings: Bank Bund). 50+. 45.202). < Seen et es 570.55 
BRIE OOOOCL FTIE) Cictc fe ce e se ee Set eo NSE eG all Ocoee ae 769.82 
MINE WOO GF UUN CMD ONG).a.pc ue stave iaid arate st Rul oeucl el Re. eae 1,000.00 


2,346.37 $2,346.37 


Matcamcashronrhan dis ct araticncart aocG cen Laake Oe Ee Ag son MA 2,603.00 


The treasurer was directed to ascertain the cost of insuring the 
stock of the Club’s periodicals which are stored in the basement 
of the library. 

The report of the editor, A. W. Evans, was read by Dr. M. A. 
Howe. This report was accepted. 

Mr. Norman Taylor gave a brief report as editor of TORREYA 
and Dr. M. A. Howe reported upon his work as delegate to the 
council of the New York Academy of Sciences. 

Dr. Howe brought up the question of the publication of a 
paper offered by Dr. F. W. Pennell for publication as a Memoir 
of the Club. A motion was made by Mr. Taylor to refer the 
question to the Budget Committee and to the Editorial Board 
for their joint consideration and report. The motion was 
carried. 

Election of Officers——The following officers were elected for 
the ensuing year: 


President, H. M. Richards. 


Vice-Presidents, John Hendley Barnhart, 
C. Stuart Gager. 


Secretary and Treasurer, Bernard O. Dodge. 
Editor, Alex. W. Evans. 


82 


Associate Editors, 


Jean Broadhurst, M. Levine, 
-eAeblanris: George E. Nichols, 
Marshall Avery Howe, Arlow B. Stout, 


Norman Taylor. 


Delegate to the Council of the New York Academy of Sciences, 
M. A. Howe. 
The president appointed the standing committees for the year. 
A list of these committees is regularly published in ToRREYA. 
Adjournment followed. B. O. DonDGE, 
Secretary. 
JANUARY 30, I9I9 
The meeting was held in the Morphological Laboratory of 
the N. Y. Botanical Garden at 3:30 P.M. President Richards 
presided. There were 17 persons present. 
The minutes of Jan. 14 were read and approved. 
The following report of the Budget Committee was read and 
adopted: 
Report of Budget Committee, 1919 
The Budget Committee of the Torrey Botanical Club met at 
the New York Botanical Garden at 2 P.M., on January 29, 1919. 
Present, Drs. Barnhart (chairman), Britton, Dodge, Evans, 
Harper, Howe, Richards and Rusby. The following budget 
was suggested for the year I9I9: . 


Estimated Income Estimated Outgo 

IDITGI OH Ss cde GeO ARERR TENSE ie $1,000 Bulletin xc hs. oe $1,400 
Sustaining members.......... 100 MORREVAjS% fort os oc ae a Ee 525 
Brlletiny sh eae skies ees. Ss es 750 Memoirs (2.03) s 022s. (eee 000 
POLLEY Areierete ee tes Oras weet 180 Indexcardsa- sone. eee 200 
INVERT OIGS tree rarer Tonons sxe ostoto 1p 100 Secretary-Treasurer.......... 300 
Advertisements.............. 50 Sundries: .:. 2 cnc. ca ee Weep 
Indexicardsiys,ccyias favenle see 200 Totaly: ks Bs. $2,545 
INEELESER ete sesscicicne eietalen ites 90 
SLIM GTICSE ti cnustj-cskeneee tiene aie 75 

Ota lesa eeve easier ees eae $2,545 


Respectfully submitted, 
MarsHALL A. HOWE, 
Secretary. 


83 


Dr. Barnhart, chairman of the Budget Committee, reported 
that all members of the committee were present at the meeting. 

The treasurer was authorized by vote of the Club to insure the 
stock of the Club’s publications, against loss by fire and water, 
for four thousand or five thousand dollars. 

Dr. Britton moved to appoint Dr. M. Levine, business manager 
of the Club’s publications for purposes of increasing advertising 
and circulation. Motion carried. 

Dr. Pennell reported that the Auditing Committee had ex- 
amined the books of the treasurer and had found them to be 
correct. 

The scientific program was then in order. The program 
consisted of ‘‘Abstracts and Criticisms of Botanical Papers read 
at the Baltimore meeting of the A. A. A. S.”’ 

Prof. R. A. Harper, Dr. E. W. Olive and Dr. A. Gundersen 
each reported on several papers which he had heard read. 

Discussions followed. 

The meeting adjourned at 5 P.M. 

B. O. DopcE, 
Secretary. 
A CORRECTION 

Syntherisma pruriens, error in publication. Byan unfortunate 
slip of the pen in transferring Panicum pruriens Trin. to another 
genus in the preceding March number of ToRREYA (19: 48. 14 
May 1919) the generic name was made to read “Sanguinale.”’ 
This orthographic error should be corrected to Syntherisma 
pruriens (Trin.) nom. nov., the date of publication remaining 14 
May IgI9, the actual date of issue of the March number of 
the journal.—J. C. Arthur. 


NEWS ITEMS 


Dr. William S. Cooper, of the University of Minnesota, 
expects to spend the summer in a study of the ecology of the 
dunes at the mouth of the Salinas river, near Monterey, Cali- 
fornia. As the climax vegetation of these dunes is chaparral, 
Dr. Cooper’s work will be an extension of his former study of 
that formation. 


84 


The Ecological Society of America will hold a meeting at the 
Throop College of Technology, Pasadena, California, on June 
Ig, 20 and 21st. A joint session for the reading of papers of 
general interest will be held with the Western Society of Natural- 
ists. Field trips have been arranged to Mt. Wilson and to the 
fossil deposits at Rancho La Brea. 


The Ecological Society of America announces in its Bulletin 
the appointment by the president, Barrington Moore, of a ‘‘ Com- 
mittee on Cooperation.’’ The aim is to further different phases 
of ecological work by combined effort ona concrete problem and 
to suggest a list of problems where such co-operation would 
prove of value. The problem decided upon is ‘‘ The factors 
limiting distribution on the mountains in the northeastern 
states.’”’ The members selected represent the three main lines 
of work of the society, plant ecology, forestry and zoology. 
They are: for plant ecology, H. L. Shantz of the Bureau of 
Plant Industry, Washington, D. C., and Norman Taylor of the 
Brooklyn Botanic Garden; for forestry, George P. Burns of the 
University of Vermont, Burlington, Vt., and Barrington Moore 
of the American Museum of Natural History, New York; for 
zoology C. C. Adams of Syracuse University, and one other not 
yet appointed. During the first week in June, Messrs. Moore, 
Adams and Taylor visited Mt. McIntyre and Mt. Marcy in the 
Adirondacks, and a more extended trip of the whole committee 
is scheduled for July. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of ToRREYA in which their papers appear, will kindly notify the 
editor when returning proof. 

Reprints should be ordered, when galley proof is returned to the editor. The 
New Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
following rates: 


2pp 4pp 8pp 12pp 16pp 20pp 
25 copies $ .79 $1.14 $1.78 $2.32 $2.87 $3.28 

50 copies 1.03 1.43 2.23 2.82 3.52 3.92 
100 copies 1.45 2.03 2.73 3.50 4.23 4.55 


200 copies Daly 3.24 3.92 5 25 6.52 6.92 
Covers: 25 for $1.00, additional covers 114 cents each. 
Plates for reprints, 50 cents each per 100. 


Committees for 1919. 


Finance Committee Program Committee 
R. A. Harper, Chairman. Mrs. E. G. BRITTON, Chairman: 
J. H. BARNHART, PrRoF. JEAN BROADHURST 
Miss C. C. HAYNES B. O. DopGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F. J. SEAVER 
J. H. BARNHART, Chairman, Membership Committee 
R. A. HARPER J. K. SMALL, Chairman. 
N. L. BRITTON T. E. HAZEN 
A. W. Evans E E. W. OLIVE 
M. A. Howe Local Flora Committee 
H. H. Russy N. L. Britton, Chairman, 
Field Committee Phanerogams: Cryptogams: 
F.W. PENNELL, Chairman. E. P. BICKNELL Mrs. E. G. BRITTON 
Mrs. L. M. KEELER N.L. BRITTON T. E. Hazen 
MICHAEL LEVINE C. C, CurRTIS M. A. Howe 
GEORGE T. HastTIncs K. K. MACKENZIE MICHAEL LEVINE 


PERCY WILSON NORMAN TAYLOR W.A. MuRRILL 
F. J. SEAVER | 
Chairmen of Special Committees on Local Flora 
Feris and Fern Allies: R. C..Benedict. Lichens: W.-C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H.. M. 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti:’ H. M. Richards, F. 
Except Russula and Lactarius: hiss G. Seaver, Mel T. Cook 
-- Burlingham ~~ Oomycetes: C. A. King 
Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 
Polyporeae: M. Levine Chytridiaceae, 
_ Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurst 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


OTHER PUBLICATIONS 


OF THE 


TORREY BOTANICAL CLUB 


| (1) BULLETIN 

A monthly journal devoted to general botany, established 
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| Vol. 19 May, 1919 No. 5 


- TORREYA. 


A Monraiy Journat or Boranicat Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873 


CONTENTS 
* > A New Rictcia from .Peru: ALEXANDER “‘W. EVANS. 2.05) ciecd levnscane csp 20s uetponsserarss 85 
Whats: Ecology: Hi. AY GLEASON 4s bec) op pan teale ce da deet-ogtebs gehen ae dete dageyg oer E wae ds 89 
AwNvewCalifornia-Cypressi; bL. Rs ABRAMS (3-5: (25). cage. Fates be Nee Eats vemos ate Fea eee g2 
\ Reviews: : 

Macfarlane’s Causes and Course of Organic Evolution: C. Stuart GAGER....-: 93 

The Swiss League for the Protection of Nature: E. G. BRITTON.....-..-.....2+. 101 
Proceedings of the Club ....... Se RR ee ark Depaed er AEA Neos aoe Ube pp ch» Lip aeae E Sign Seabees 102 
sg 18 BC 7 TA 8 a ee NE Pen SE? | ee? Se ated Ws Rea SUG ee, UR oats aoe ka hee 105 

‘ PUBLISHED FOR THE CLUE 
} AT 41 NortTH Queen Street, Lancaster, Pa 


sy THe New ERA Printinc ComPrany 
“Entered ar the Post Office at Lancaster, Pa., as second-class matter. 


THE TORREY BOTANICAL CLUB | 


OFFICERS FOR 10919 


President 
H. M- RICHARDS, Sc.D: 
Vice- Presidents. 


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€. STUART GAGER, PH.D. 


Secretary and Treasurer : 
BERNARD O. DODGE, Pu.D. 
CoLuMBIA ‘UNIVERSITY, N. Y. City. 
Editor 
ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


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J. A. HARRIS, Pu.D. G.E, NICHOLS, Pu-D. 
ee AVERY HOWE, Pu.D. ARLOW B. STOUT, Pu. D. 


NORMAN TAYLOR. 


Delegate to the wee of the New York Academy of Sciences 
. A. HOWE, PH.D. 


OFFICIAL ORGAN OF THE WILD FLOWER PRESERVATION 


Society oF AMERICA 


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NORMAN TAYLOR 
Brooklyn Botanic Garden 
Brooklyn, N. Y 


TORREYA 


Vol. I9 No. 5 
} May, I9I9 


A NEW RICCIA FROM PERU* 
By ALEXANDER W. EVANS 


Through the kindness of Mr. W. R. Maxon, of the United 
States National Museum, the writer has received for study an 
interesting collection of Peruvian Hepaticae, made by Messrs. 
O. F. Cook and G. B. Gilbert in 1915. One of the most re- 
markable of the species represented is the Riccia noted below, 
which seems to be undescribed. The remaining species are not 
yet wholly determined, so that a complete account of the col- 
lection can not be published at the present time. 


Riccia bistriata sp. nov. 


Plants growing in irregular patches: thallus simple or once 
or twice dichotomous, strap-shaped to obovate, mostly 0.5- 
1.5 cm. long, 2-4 mm. wide, and 9.5-0.6 mm. thick in the median 
portion, distinctly areolate and dull green above, a marginal 
band becoming bleached with age, more or less pigmented with 
purple below, especially toward the margin, median sulcus in 
the apical region only, I-1.5 mm. long, the older portions of the 
thallus plane or nearly so above and convex below, gradually 
thinning toward the margin, where the two surfaces meet at an 
acute angle; ventral scales inconspicuous, hyaline, scarcely pro- 
jecting beyond the margin; cells of the primary dorsal epidermis 
subhemispherical, the upper part soon collapsing and disappear- 
ing, leaving the basal portion in the form of a thickened shallow 
cup; green tissue of the usual Riccia type, consisting of upright 
rows of cells separated by narrow (usually) four-sided canals 
not constricted at the dorsal surface of the thallus, each row of 
cells usually connected longitudinally with four other rows and 
composed of five or six cells, the longitudinal walls common to 
two rows being marked by two colorless bands, of thickening 


* Contribution from the Osborn Botanical Laboratory. 
(No. 4, Vol. 19 of ToRREYA, comprising, pp. 57-84, was issued 25 June, 1919] 


85 


86 


extending from the compact ventral tissue to above the middle of 
the uppermost green cells, united at their upper ends and some- 
times at various points along their length; compact ventral 
tissue mostly eight to ten cells thick, composed of uniform paren- 
chyma without oil-bodies: inflorescence (so far as known) 
dioicous, the antheridia not seen: spores dark brown to almost 
black, becoming very opaque with age, more or less angular, 
110-130 pw in diameter, with a narrow, irregular and often in- 
terrupted wing-margin, 4 uw or less in width, spherical face covered 
over with a fairly regular reticulum formed by low ridges 3 u 
or less in height, the meshes mostly 10-15 pw in diameter, plane 
faces with lower ridges, usually irregular but sometimes forming 
a more or less distinct reticulum. [Fic. 1.] 


On soil, Santa Ana, 900 m. alt., June 25, 1915, Cook & Gilbert 
I48T. 

The peculiar bands of thickening which are found in the walls 
of the green cells represent a feature which has not before been 
noted in the Marchantiales. In a section cut parallel with the 
surface of the thallus (Fic. 1, D) these bands are especially con- 
spicuous. They appear in the form of minute circular structures 
situated in the walls common to two cells and projecting into the 
cavities, this appearance being due to the fact that the thicken- 
ings deposited by one cell correspond with those deposited by 
its neighbors. In most cases each cell is octagonal in section and 
is bounded by four other cells alternating with four air-canals. 
At its periphery it shows normally eight thickenings, two for 
each bounding cell. The thickenings are usually distinct and 
definitely two in number, but they sometimes have vague out- 
lines and may be increased to three. In a section cut at right 
angles to the surface of the thallus (Fic. 1, E) the true form of 
the thickenings becomes evident. They now appear as parallel 
bands, running longitudinally with respect to the rows of green 
cells. Each pair of bands begins at or near the lower end of a 
row and extends upward to the cells just beneath the epidermis. 
A short distance above the middle of these cells the two bands 
coalesce and form a narrow arch. During their course they 
sometimes unite here and there but are usually quite free from 
each other. 

Although thickened walls have not before been observed in the 


87 


green tissue of the Marchantiales, thick-walled cells of various 
types have repeatedly been noted in other parts of the thallus, - 
especially in the more complex genera of the Marchantiaceae. 


Fic. 1. RICCIA BISTRIATA Evans. 


A. Cross section of thallus in apical region, XK 22. B. Cross section of same 
thallus near basal end of median sulcus, XK 22. C. Cross section of same thallus 
in older part, X 22. D. Section of green tissue parallel with surface of thallus, 
X 300. E. Section of green tissue perpendicular to surface of thallus, showing 
bands of thickening in section and surface view, X 300. F. Spore, X 400. The 
figures were all drawn from the type specimen. 


In addition to the tuberculate rhizoids which are of almost uni- 
versal occurrence, the epidermis in many cases is distinguished 
by a definite cuticle and conspicuous trigones, while the cells 


88 


surrounding the pores sometimes show thickened radial walls. 
In the compact ventral tissue, moreover, thick-walled cells 
with elongated pits are not uncommon, and a number of species 
are known in which pointed sclerotic cells with pigmented walls 
can be demonstrated. Of course none of these cells bear much 
resemblance to the green cells of the Riccia. Perhaps the latter 
are more directly comparable with the parenchymatous cells 
found in the costa of Pellia epiphylla (L.) Corda and P. Neesiana 
(Gottsche) Limpr. Here, as in all the Jungermanniales, the 
gametotype is destitute of air-spaces, but the interior cells of 
the thallus show distinct vertical bands of thickening in their 
longitudinal walls. The bands, which are narrow and often 
pigmented, undoubtedly serve in a mechanical capacity, and 
the same thing is probably true of the much longer bands of 
Riccia bistriata. 

According to Stephani* twenty-three South American species 
of Riccia were known in 1898, thirteen belonging to Riccia 
proper and ten to Ricciella. Not one of these species is accredited 
to Peru. In 1911 Weberbauert was able to report two species 
from the vicinity of Mollendo, listing them under manuscript 
names of Stephani. Since these species have not been adequately 
published, so far as the writer knows, they need not be further 
considered. Among the species described by Stephani, R. 
Weinionis Steph., collected by Weinio at Rio de Janeiro, is 
perhaps the most closely related to R. bistriata. In the Brazilian 
species, however, the spores are smaller, measuring 102 u in 
diameter, the inflorescence is described as monoicous, and the 
dorsal sulcus is not restricted to the apical region. It is unfor- 
tunate that Stephani makes no allusion to the anatomical features 
of his species, nothing being said about the epidermis, the green 
cells, or the compact ventral tissue. 

SHEFFIELD SCIENTIFIC SCHOOL, 
YALE UNIVERSITY 


* Bull. Herb. Boissier 6: 310-343, 361-378. 1808. 
7 Engler & Drude, Vegetat. der Erde 12: 145. Io91I. 


89 


WHAT IS ECOLOGY? 
By H. A. GLEASON 


At a recent meeting of a well-known botanical society it was 
suggested somewhat jocularly that the field of plant ecology is 
not well defined, and that the speaker would welcome a further 
definition of the phases of plant life that are covered by it. Now 
the botanist who made this remark certainly does know what 
ecology is. So do also the various botanists who have made and 
are still making similar public statements on the same subject 
and to the same effect. They know from actual experience with 
the subject itself and with the men who work init. The difficulty 
is that ecology is so different from the more familiar divisions of 
botanical science, morphology, physiology, and the like, that 
some of them fail to classify the subject properly in their own 
minds. 

In order to present the matter, let us attempt a definition of 
botany, to be used as a point of departure in formulating later 
a definition of ecology.* Botany is the accumulation and or- 
ganization of knowledge of plants. This definition holds for the 
student who learns from the printed page or the observer who 
takes his knowledge directly from the plant; for the beginner 
acquiring the most elementary rudiments of the science or the 
investigator extending the limits of knowledge. Botany does 
not properly refer to the plant itself, although it is sometimes 
used in that sense. A speaker may refer to the interesting 
botany of Mexico when he really means the interesting flora. 

Morphology, as one branch of botany, may be defined by the 
addition of one limiting phrase to the definition of botany: it is 
the accumulation and organization of knowledge concerning the 
form and structure of plants. Strictly speaking, the term does 
not refer to the plant itself, yet in common usage it has frequently 
been applied in that way. For example, a teacher may ask of 
a student ‘‘Describe the morphology of the corn-kernel,’’ when 
he really expects a description of its structure. Or he writes an 
article on the morphology of the vascular bundle of corn, and 
the title is accepted without criticism as referring to the structure 


* In this connection see TORREYA for May, 1912.—ED. 


90 


of the bundle and not to our knowledge of its structure. This 
sounds like mere quibbling over the meaning of words: so it is 
introduced to show that a word originally applied to a division 
of knowledge is now applied to certain features of a plant. The 
same thing is true of physiology, of pathology, of various other 
-ologies, not merely in the general field of botany but in other 
sciences as well. 

To revert to the original subject, plant ecology may be defined 
as the accumulation and organization of knowledge concerning 
the correlation between the plant and its normal environment. 
It now becomes difficult to divert the word from the meaning 
given here into a concrete application as has been done so suc- 
cessfully with morphology and physiology, because the subject 
is based not on the plant alone, but on the plant and its environ- 
ment together. Nevertheless, the attempt is frequently made. 

A botanist announces that he is studying the ecology of Smith’s 
Bog. Narrowed down to an exact statement by careful question- 
ing, he admits that Smith’s Bog has no ecology, that he is really 
interested in the environmental relations of the plants there, 
and that he discovers these relations, at least in part, by observa- 
tions on their form and behavior. Undoubtedly the original 
statement has brevity and is clear in its meaning, but it is im- 
possible to include consistently any measurable or visible process 
or structure in a plant exclusively under the. term ecology. 

Two common expressions of this correlation between plant 
and environment are found, as just stated, in the structure and 
behavior of the plant. They must be studied by the methods 
of morphology and physiology, they must be described in the 
same terms used in morphology and physiology, yet the result 
of the study is neither: they deal with the structure and behavior 
of the plant, the result deals with the correlation between its 
structure and behavior and the environment. The elongation 
of the dandelion scape is a study in physiology, the structure and 
development of the pappus a study in morphology, the dissemi- 
nation of the dandelion a study in ecology. But since the ob- 
servable effect of the interrelation of plant and environment is 
frequently termed the morphology or physiology of the plant, 


91 


there is a not unnatural tendency on the part of morphologists 
and physiologists to consider ecology, or at least this part of it, 
as equivalent to or included in their own subjects. Since these 
subjects have accepted names, they ask ‘‘ What is ecology?” 

Another expression of the interrelation between plant and 
environment is seen in the restriction of a species to a particular 
type of environment, that is, to a particular habitat. This 
phenomenon can not be observed on a single individual, which is 
of course restricted to a single station, but must be studied from 
many individuals of one race. In this case the visible result is 
apart from either morphology or physiology, and to some botan- 
ists this alone is ecology, just as the behavior of a plant is physi- 
ology. But after all, the habitat-relation of a species is only 
one type of behavior, dependent upon the physiological functions 
of the single individual, but measured and tested by the behavior 
of many individuals or of the race. 

It is hardly necessary to say that tangible or visible phenomena 
are frequently noticed before the underlying processes or correla- 
tions are discovered. Starch was known before photosynthesis; 
growth of trees before cambium. The morphological effect of 
ecological relations, such as alpine dwarfing, was known before 
the causes, which are even yet not fully understood. Plant 
associations were described long before their fundamental nature 
Was appreciated. 

In conclusion, let it be repeated that ecology is a division of 
knowledge, to be studied only through perceptible phenomena, 
which are frequently structural or functional in nature and there- 
fore subjects for morphology and physiology also, but that the 
questions which ecology seeks to answer, the knowledge which 
it aims to supply, deal not with structure and function alone 
but with the correlation between the plant as a whole and the 
environment in which it grows. 


NEw YorK BOTANICAL GARDEN 


: 


92 


A NEW CALIFORNIA CYPRESS 


Cupressus nevadensis sp. nov. 


By L. R. ABRAMS 


Small tree attaining a maximum height of 20-25 m. and a 
diameter of 6-8 dm., with spreading branches forming a broadly 
conical crown. Bark fibrous, longitudinally fissured, 15-25 cm. 
thick, reddish brown within, weathering light gray-brown on 
the exposed surface. Leaves light green and somewhat glaucous, 
closely imbricated on the slender distinctly 4-angled branchlets, 
1.5 mm. broad, sharply acute and keeled, with a conspicuous 
active dorsal resin duct. Cones solitary or clustered, broadly 
oblong to subglobose, 20-25 mm. long about 20 mm. broad, 
light gray with a brown undertone; scales 6-8, rugosely roughened 
with the wrinkles converging at the umbo, the upper lateral 
longer than broad and acute at the upper angle; umbose on the 
lateral scales near the apex, scarcely pointed, those of the upper 
pair elevated and pointed; seeds numerous, 4-5 mm. long, light 
brown tinged with purple and somewhat glaucous, rugosely 
wrinkled and sparsely papillate; hilum oblong-oval. 

In its resinous character it suggests Cupressus Macnabiana 
Murr., but the larger cones and glaucous seeds show a closer 
relationship to Cupressus Sargenti Jepson of the California Coast 
Ranges. 

This species, the first to be reported in the main Sierra Nevada, 
was first discovered by Mrs. Leo Polkinghorn in 1907, who for- 
warded specimens to the late Professor W. R. Dudley. In 1915, 
recognizing the peculiarities of these specimens, the writer 
visited the grove for further material and notes on the living 
trees. It grows on Red Hill, Piute Mountains, near Bodfish, 
Kern County, at an elevation of 5,000 to 6,000 feet. Associated 
with the California juniper, blue Oak, digger pine, and such 
desert plants as Pinus monophylla and Ephedra viridis. Type: 
Abrams 5308, July 29, 1915. 


STANFORD UNIVERSITY 


93 


REVIEWS 
Macfarlane’s the Causes and Course of:Organic' Evolution * 


This is an unusual book in several particulars, and notably in 
its wide scope, covering nearly the entire field of evolution on 
the earth, from “Ether and Energy in the evolution of matter”’ 
(Chapter I) to such topics as ‘Morals as a factor in organic 
evolution and their biological origin’? (Chapter XXIII), ‘‘Re- 
ligion as a factor in human evolution”’ (Chapters XXIV-—X XVI), 
“Human organization in relation to environment” (Chapter 
XXIX), and “Probable future advances in human evolution”’ 
(Chapter XXX). Chapters I to VIII deal with the evolution 
of energy and of matter, inorganic and organic; Chapter IX with 
the idea and term (first elaborated and used by this author) of 
“Proenvironment’’; Chapters XI—XIII with ‘‘The evolution 
of plants’; Chapters XIV-XVIII with “The evolution of 
animals’’; and Chapters XIX—XXX with the evolution of man 
and questions closely connected therewith in the realms, not 
only of the physical, but of the intellectual, moral, religious, and 
social. 

It is unusual to find a recent book dealing with the evolution 
of plant and animal forms, and having only 28 illustrations; 
and equally unusual to find a book of such pretensions as this 
one disregarding, or considering only briefly or incidentally, some 
of the working hypotheses that loom largest in contemporary 
research and in recent scientific periodicals and other publi- 
cations—such hypotheses as, for example, the mutation theory 
and Mendelism, and the recent work in genetics, and eugenics. 
This is in harmony, however, with what appears to be the author’s 
attitude toward some of this later work. For example, noting 
that Mendel and ‘‘nearly all of his followers have treated of 
naked eye appearances”’ to the neglect of cytological details, 
and referring to his own well known study of “‘unisexual and 
bisexual heredity’’ (1883), where ‘‘there is no dominance or 
recessiveness shown,” he ‘‘considers that most of the cases of 

* Macfarlane, John Muirhead. The causes and course of organic evolution. 


A study in bioenergetics. New York, The Macmillan Co., 1918. Pp. i-ix + 875. 
28 figs., three colored plates, and one uncolored. $4.00. 


94 


‘Mendelian inheritance’ in plants and animals will probably be 
found to conform to such conditions, where they have been 
studied microscopically.’”’ This not only implies that dominance 
and recessiveness are the essence of Mendelism, as conceived by 
present day geneticists, but is also contrary to certain published 
results of Mendelian studies. It must be kept in mind that 
macroscopic characters (e. g., color and coloration) are often mass 
effects of histological detail. In fact, the author states definitely 
his opinion “‘that most of the discussion on the possible acquisi- 
tion of new characters, on the hereditary transmission of such, 
on dormant (sic) and recessive factors, have mainly been of value 
in stimulating research” (p. 150), and he considers that “varietal, 
specific, generic, and wider characters resolve themselves into 
the waxing or waning of definite substances, according as en- 
vironal stimuli act on certain constituents of the cells.” 

The keynote of the volume, as stated in the preface, is that 
“energy, continuity, evolution may be said to constitute the triune 
basis of existence’’; and, further on (pp. 170-171), that “Rela- 
tive distribution and relative condensation of energy .. . are 
the important factors at the foundation of all organic as of all 
inorganic changes.’’ In fact, the viewpoint throughout, as the 
subtitle would lead one to expect, is that of energy, rather than 
form, and the elaboration of this conception involves the use of 
an unfamiliar nomenclature, originating with the author, and 
running throughout the book. Thus, “in passing from the 
inorganic crystalloids and colloids to those composing organic 
bodies, the fundamental need of the case was the evolution and 
increasing activity of an energy that would as far excel electricity 
in its perfect quality as does the latter excel chemical affinity, 
and it again heat” (p. 77). Heat, light, chemical affinity and 
electricity, as phases of energy, have been unequal to the task 
of energizing ‘‘the inert ether particles that form the centers of 
the atomic and molecular structures”’ (p. 81) and the author 
formulates it as a working hypothesis, ‘‘that the transition from 
the inorganic colloid to the organic colloid body was gradually 
accompanied by the evolution of a new and more condensed 


(Dp. 33):, Janome 


’ 


phase or modification of energy, the ‘bzotic 


95 


energy is ‘‘the basic energizer of organisms,’’and its “forerunner 
and anticipator’’ was ‘‘a redistribution of electric energy,” 


‘ 


which ‘‘distinguished chemists’’ consider ‘‘can be traced round 
each molecule”’ (p. 81). Biotic energy is ‘‘a more condensed, 
perfect, and powerful type of the all-pervading energy than even 
electric’’ (p. 26). The reviewer does not quite understand how 


ae 


one kind of energy can be more ‘“‘perfect’”’ than another. This 
adjective is frequently used throughout the book in comparing 
various kinds of energy (pp. 800-805). What is a “perfect” 
form of energy? How any of the lower forms of energy are con- 
verted into biotic energy is not known (p. 102). 

Eight different kinds of energy are enumerated, viz., thermic, 
lumic, chemic, and electric, acting in non-living bodies; and 
biotic, cognitic, cogitic, and spiritic, acting only in living bodies. 
Biotic energy energizes protoplasm (7. e., cytoplasm); cognitic 
energy energizes chromatin, it underlies the phenomena of ir- 
ritability, awareness, response, and _ sense-perception. Cell 
division is ‘‘due to steady discharges . . . from the center of 
the nucleus or the nucleolus of cognitic energy,’ and conjugation 
“seems to be due to the establishment of unlike or differently 
charged amounts of cognitic energy,” etc. In fertilization the 
“mutual’’ attraction of sperm and egg is not due to their mole- 
cules ‘‘as physical entities,’’ but to definite discharges of chemic, 
electric, biotic, or other energies that transverse the particles,” 
etc. Cogitic energy energizes the substance of the nerve ganglia 
(Nissl substance, neuratin). It is a ‘‘more perfect” (p. 801) 
form of energy than cognitic, and enables ‘“‘organisms to form 
more complex and interlocked impressions of a mental kind”’ 
(p. 801). ‘‘There evidently exists a more complex form of 
energy than the biotic, cognitic, or even cogitic, and which we 
have termed the spiritic’’ (p. 801); and there is probably a speci- 
ally complex substance in “the gray frontal matter of the brain, 
and which hypothetically we may call spiritin”’ (p. 804). 

We have given considerable space to this unique conception 
and terminology because it is the unifying thought running 
throughout the book, and indicates the angle from which the 
entire question of evolution is conceived and discussed by the 


96 


author. Without implying any real analogy, one cannot help 
but recall here Harvey’s statement in his epoch-making book, 
‘““The motion of the heart and blood in animals,” viz: ‘“Fer- 
nelius, and many others, suppose that there are aerial spirits 
and invisible substances . . . but Medical Schools admit three 
kinds of spirits: the natural spirits flowing through the veins, the 
vital spirits through the arteries, and the animal spirits through 
the nerves; . . . but we have found none of all these spirits by 
dissection, neither in the veins, nerves, arteries nor other parts 
of living animals.’ One is also reminded here of the primordial 
units of “mind-stuff,”’ in which Clifford believed, though on 
evidence (so James tells us) that seemed quite worthless to Bain. 
It seems to the reviewer as though the author were reviving for 
the microcosm a conception analagous to that formerly held of 
the macrocosm, but long since abandoned in the light of the 
scientific investigation and interpretation of nature. The 
ancient polytheism, for example, postulated a spirit presiding 
over every natural process, and over every act of daily life—a 
god of the east wind, and of the west wind, of the sea and of the 
depths of the earth; a god of going out, and a god of returning 
home, a god of planting, and a god of harvest. So the book under 
review postulates a special kind of energy for the various kinds 
of functions, and each kind differs from all the other kinds in 
its “‘perfectness.”’ A botanical reviewer may prudently re- 
frain from a critical discussion of the purely physical question of 
kinds and qualities of energies, but it would be interesting and 
no doubt profitable, to hear what comments a physicist would 
make. An acceptance of the author’s theory would demand a 
considerable readjustment of the mode of thought of contempor- 
ary experimental physiologists. 

Another idea to which the author assigns much prominence 
and for which he coins a new term (as noted above), is “‘proen- 
vironment’? (Chapter IX, and passim). “This is defined (p. 242) 
as ‘that great and ever-expanding law of organic life, by which 
varied environal stimuli are linked into a summated and uni- 
fied response, that brings each organism into satisfied relation to 
the environment;” or again (p. 629), “the capacity of an or- 


97 


ganism for perceiving and then positively growing or moving 
toward an environment that is the most satisfying for it.” The’ 
various tropisms, and the response of Mimosa leaves to shock are 
acts of proenvironment. ‘In all moral acts, as in simpler and 
more primitive actions and reactions amongst plants and ani- 
mals, the fundamental outcome of moral response is a satis- 
fied state’ (p. 664). ‘‘Moral attitudes all represent proen- 
vironal efforts by individuals” (p. 656). ‘Enterprise is varied 
and vigorous proenvironal planning that is being put into prac- 
tice’ (p. 641). ‘“‘Sex fusion is a proenvironal act”’ (p. 789). 
“So the building of nests above ground, the excavation of nests 
below the surface, or the hollowing of trees into nests by ants and 
other insects; the gradual elaboration of complex log houses and 
dams by beavers; the planning and erection of a lake dwelling 
by medieval man are all proenvironal acts,” etc. (p. 790). ‘‘Man- 
kind has proenvironed the law, “‘Thou shalt love thy neighbor 
as thyself’”’ (p. 791). The idea of proenvironment, or something 
closely akin to it, was proposed by Cockayne and Foweraker in 
their paper on ‘“‘The principal plant associations in the immediate 
vicinity of Canterbury College Mountain Biological Station”’ 
(Trans. New Zealand Inst. 48: 166. 1916). The term there 
proposed was Epharmonic variation, which was defined as ‘a 
change in its form of physiological behavior beneficial to an 
organism, evoked by the operation of some environmental 
stimulus.’’ For the intellectual realm the idea is also stated by 
James in ‘‘The Will to Believe,’’ where he says (p. 76): “. .. 
of two conceptions equally fit to satisfy the logical demand, that 
one which awakens the active impulses, or satisfies other aesthe- 
tic demands better than the other, will be accounted the more 
rational conception, and will deservedly prevail.’’ The con- 
ception, however, appears to have been nowhere so thoroughly 
elaborated as by the author under review. 

In Chapter VIII the author postulates the law of ‘‘Pen- 
tamorphogeny,”’ that is, that there are five factors or cooperative 
agents in organic evolution, namely, heredity, environment, 
proenvironment, selection, and .reproduction (p. 204). This is 
somewhat in contrast to Osborn’s law of ‘‘Tetraplasy,”’ the 


98 


“four inseparable factors of evolution” (heredity, ontogeny, 
environment, and selection). Macfarlane rejects ontogeny as a 
cause or factor in evolution. 

In accepting the hypothesis “‘that living and non-living bodies 
are alike irritable’ (p. 44), no reference is made to Bose’s full 
development of that idea in his Response in the Living and Non- 
living, and other writings. 

On page 81 “inert ether particles” are referred to as forming 
“the centers of the atomic and molecular structures.” No 
reference is here made to the electron theory of atomic structure, 
which regards the atom as, in figurative sense, a miniature ‘‘solar 
system,’ with negative electrons moving in orbits around a 
nucleus of positive and negative electrons—chiefly positive. This 
hypothesis, based upon studies in radioactivity and related in- 
vestigations, has been the one in most general favor with physi- 
cists for a decade orso. Attention may also be called here to a 
present tendency of some physicists to question the older con- 
ception of a universal elastic ether, in light of the theory of 
relativity, which originated in the famous experimentum crucis 
of Michelson and Morley (1887) to obtain evidence of an ether 
drift.” In fact, a physicist friend has assured the reviewer that 


”) 


the expression ‘“‘inert ether particles’? does not convey any 
meaning to a physicist. 

Adhering to the energy point of view, and the point of view of a 
granular or atomic ether, protoplasm is defined (p. 86) as “a 
definitely correlated rotatory motion of variously energized 
(or linked) and highly complex groups of ether particles of col- 
loid nature, in which the specific rates of motion between the 
This would seem to 
define protoplasm as a mode of motion rather than as a substance. 
In harmony with this conception, life is defined (p. 97), as 


“Relatively similar complexity and synchronism of motion of 


b] 


groups are an expression of biotic energy.’ 


quinary, hexary, and heptary compounds, that represent similar 
complex definiteness of structure and similar lines of flow of 
biotic energy.” 

The different tropisms shown by living organisms depend each 
upon a special class or kind of plastids or energids which ‘‘show a 


99 


special sensitivity and polarity to environal stimuli (p. 121); 
these plastids evolved in the probable order of leucoplastids” 
(chemoenergids), helioplasts (chromoplasts and _ chloroplasts) 
or photoenergids, geoplasts (geoenergids), thigmoplasts (me- 
chano-energids), and parohelioplasts, which 
their energizing results, not as yet as definite structures. Thus 


‘ 


‘are only known in 


for every class of physiological function there is postulated by 
the author, not only a particular kind of energy, but also a 
particular structure. Some of these structures are known 
only by inference from a given function. This granular philos- 
ophy is extended to include the notion that there is ‘‘a large 
series of bodies common to all plants . . . which can at any 
time be gradually reproduced by the joint action on, and re- 
action of protoplasm and its related ferments under the more 
fundamental action of appropriate environmental stimuli.”’ 
These bodies may at times be reduced to ultra-microscopic 
bodies (p.150). This conception would appear to be a form of, 
or analogous to, pangenesis. Its acceptance, according to the 
author, leads logically to a rejection of the concept of ‘‘acquired 
’ and therefore the troublesome problem of the 
inheritance (or otherwise) of acquired characters vanishes. 

In the discussion of heredity, on pages 175-179, no reference 
is made to much modern work—Spencer’s definition, for example, 
being quoted, but no reference made to Johannsen’s fruitful 
definition and studies. Johannsen’s definition, ‘the appear- 
ance, in successive generations, of the same genotypical con- 
stitution of the protoplasm,” is suggested by the author’s 
definition: ‘‘the like continuity of molecular structure in relation 
to like outgoing and incoming currents of energy, so long as a 
body is exposed to the same environment, or to an environment 
that, within definite limits, fails to alter its average constitu- 
tion” (p. 179). This definition involves the conception that 
variation, or disturbance of heredity (p. 178) is ‘‘due to changed 
environal condition,’ which is the prevailing conception of 
geneticists as to the cause of variation. On page 187 both 
heredity and variation are defined in terms of energy. 

The theory is maintained (p. 301, and elsewhere) that “‘the 


characters,’ 


100 


simpler animals evolved as offshoots from colorless bacterial 
lines of plant organization. A review of the chapters on animal 
evolution is not here attempted. 

The statement that, when spores mature, ‘they throw off 
and break down so much chromatin material” (p. 335), is apt 
to mislead, if indeed it is not incorrect as referring to the reduction 
division resulting in the haploid number of chromosomes. 
The phenomenon of alternation of generations is erroneously 
limited to ‘‘classes of plants higher than the algae” (p. 336), 
Hoyt’s work with Dictyota, Harper’s with Ascomycetes, and 
Blackman’s with rusts, for example, being overlooked. In the 
genealogical tree (facing page 356) the now generally recognized 
group, Cycadofilices, does not appear to be mentioned. The 
hypothesis that monocotyledons and dicotyledons “all sprang 
from the great Cordaital stock” (p. 367) is at variance with a 
mass of evidence and opinion to the effect that the Cordaitales 
are not in the ancestral line of the angiosperms at all, but only’ 
of the gymnosperms. 

Pages 598 to 850 of the book are devoted to psychological, 
archaeological, anthropological, religious, and sociological ques- 
tions of which only brief mention can be made in a botanical 
magazine. It is interesting to note that the author postulates 
morality for the lower animals (p. 660). ‘‘Why,” he asks, 
“‘should the maternal care of the bird . . . be denied the praise 
of being moral?”” That morals ‘do not originate with man . 
is clearly shown by the many moral acts of bees, beavers, crows, 
ants, and apes.” In Chapter XXVII on ‘“‘The competitive 
system amongst the lower animals and with man,’’ the social sym- 
pathies of the author seem to be indicated by the dark picture 
which he draws in the following quotation (p. 764): ‘The papers, 
the press, the universities and the churches are nearly all com- 
fortably subsidized in diverse and skillful ways, im order that 
they may support ‘the system.’” (The italics are the reviewer's.) 
This is not the place to discuss such statements, nor perhaps 
even to refer to them, except that they tend to inspire confi- 
dence, or otherwise (according to the reader’s own convictions), 
in the author’s judicial attitude of mind, and the logicalness of 


101 


his conclusions with reference to purely botanical or zoological 
questions. P 
The book is a very thoughtful, sincere, and scholarly treat- 

ment of the entire range of evolutionary thought. 
C. STUART GAGER 


The Swiss League for the Protection of Nature * 


A delightful book has been published in England and translated 
into French, giving descriptions and illustrations of the Alpine 
Flora of Switzerland. The pictures include snowy peaks and 
evergreen slopes and are in the daintiest pastel colors, tinged with 
the blues and purples of the distant views, and in the foreground 
beautiful with charming groups of alpine flowers, filling the 
slopes and meadows, clinging in crevices of steep cliffs and rocks 
and filling the spaces among the stones of the dangerous moun- 
tain trails. Here will be found in April, the hepatica and the 
crocus, or the primroses with the Matterhorn in the distance 
and the gentians at the foot of the glaciers; in June the anemones 
and spikes of purple orchids, wild geraniums and globe flowers; 
the edelweiss and Alpine rose with marguerites, hawkweed, and 
rampion filling the alpine meadows in July; lovely ravines, 
fringed with evergreens, with a gorgeous carpet of rainbow 
colors in the foreground melting off into the pale blues and 
snowy peaks of the dim distance. 

One of the chapters is devoted to the work which has been 
accomplished in the last twenty years by the Swiss League 
for the Protection of Nature, of which M. Henry Correvon is the 
president. The League has been instrumental in setting aside sev- 
eral alpine gardens as sanctuaries for animals and plants and a 
most interesting account may be found of its experiences with the 
tourists on whose favor and numbers the prosperity of Switzer- 
land so much depends. Instructions are given to the guides to 
prevent depredations, but sometimes even they have to look the 
other way and ignore the peccadilloes of rapacious tourists (‘‘touris- 

* Sur L’Alpe Fleurie, Promenades Poetiques et Philosophiques dans les Alpes 
par G. Flemwell, adapté de L’anglais par L. Marret et L. Capitaine, Avec 63 


illustrations dont. 20 planches hors texte en couleurs. Soc. D’Edition des Sci- 
ences Naturelles. L. Marret et Cie, Paris. May, 1914. 


102 


tes-arracheur’’). By dint of ‘“‘sweet persuasiveness and moral 
arguments”’ they have arrived at a happy solution and are plac- 
ing signs in all hotels and pensions, exhorting them to spare the 
fauna and flora. ‘‘If some people consider this an attack on their 
‘liberty’ they are giving a false interpretation to this word; for 
the society attacks neither a sane joy nor the elements of true 
liberty; it attacks only license. It fights for law and order; 
without them there is no true liberty. Without the ‘League for 
the Protection of Nature’ the edelweiss would have disappeared 
from around Zermatt as the chamois has from around Chamonix. 
Here is the lesson of history, history that repeats itself, whether 
in the jungles of Asia or the forests of Africa; and which has neces- 
sitated the creation of preserves for the fauna and flora, similar to 
the ‘national parks’ of America; the history which has led to the 
closed season in the shooting of birds and game and necessitated 
the creation of ‘gardens of refuge’ for the alpine flora of Switzer- 


lenders 
E. G. BRITTON. 


PROCEEDINGS OF THE CLUB 
FEBRUARY II, I9I19 


The first meeting in February was held at the American 
Museum of Natural History. President Richards called the 
meeting to order at 8:15 P.M. There were 28 persons present. 

No business was transacted. 

Dr. E. W. Olive gave an illustrated lecture on “‘Some. Plant 
disease survey work in New York, Virginia and Pennsylvania.” 
The following abstract was prepared by the speaker: 

The speaker spent the summer of 1918 in plant disease survey 
work, codperating with the offices of the Plant Disease Survey 
and Cereal Disease Investigations, of the U.S. Department of 
Agriculture, and with the state departments of plant pathology 
of various experiment stations. 

The special lines of investigation taken up in New York in- 
cluded studies on the prevalence of fruit diseases, of oat and 
barley smuts, of onion smut and other truck crop diseases in 


103 


the Hudson River Valley. In Virginia, the special problem was 
the determination of the extent of prevalence of a newly dis- 
covered serious disease affecting wheat, causing galls of the” 
wheat grains. 

In Pennsylvania, the work was on another recently discovered 
and very serious disease,’ the wart-disease of the potato. Al- 
though these two diseases seem to be fairly well established in 
restricted localities, vigorous measures for control and eradica- 
tion, including strict quarantine against the shipment of these 
crops outside of the area in which they now prevail, have been 
instituted by both federal and state agricultural authorities. 

Adjournment followed. B. O. DonceE, 

Secretary 
FEBRUARY 26, I9I9 

The meeting was held in the Morphological Laboratory of the 
New York Botanical Garden. Dr. Barnhart called the meeting 
to order at 3:30 P.M. There were 18 persons present. 

Mr. R. W. Woodward, 22 College St., New Haven, Conn., was 
nominated for membership by Prof. Evans. The treasurer 
reported upon the probable cost of insuring the stock of the 
Club’s publications. 

Prof. Harper called the attention of the club to a set of botani- 
cal notes taken by Prof. Newberry while attending the university 
at Paris a number of years ago. These notes were presented by 
Prof. Kemp through Prof. Harper to Dr. Britton. Dr. Britton 
responded briefly in accepting these valuable notes and promised 
te report upon them further at a later date. 

The resignations of Dr. A. H. Chivers and Mrs. W. E. Damon 
were read and accepted. 

Mr. Woodward was then elected to membership. 

The scientific program was then in order. Dr. J. K. Small 
and Dr. N. L. Britton presented a joint paper on ‘‘The Prickly 
Pears of the southeastern United States.’’ This paper was illus- 
trated with photographs and living plants. 

After adjournment, Dr. Britton led a party through the 
gardens, inspecting the Japanese witch-hazels which are in bloom. 
Meeting adjourned at 4:45 P.M. B. O. DonGeE, 

Secretary. 


104 


MARCH II, 1919 

The meeting was held at the American Museum of Natural 
History. President Richards called the meeting to order at 
8:15 P.M. There were 57 persons present. 

The Club voted to authorize the program committee to call 
the second meeting of the Club in March on Tuesday evening, 
March 25, instead of Wednesday. 

No other business was transacted. 

The program for the evening consisted of a ‘Symposium and 
Conference on Botanical Education in the Secondary Schools.” 
The following is a list of the speakers with the title of the paper 
read by each: 

Dr. Otis W. Caldwell, Lincoln High School, Teachers College. 
“Present Tendencies in High School Botany.” 

Dr. Francis I. Hughes, Boys’ High School, Brooklyn, N. Y. 
“Botany in City High Schools.” 

Dr. Cyrus A. King, Erasmus Hall High School, Brooklyn. 
“Changes in the Teaching of Botany and Biology in the High 
School.”’ 

Dr. Paul B. Mann, The Evander Childs High School. ‘“‘The 
Relation of First Year High School Botany to Advanced Work 
with Reference to Certain Applications and By-products.”’ 

Dr. C. Stuart Gager, Director of the Brooklyn Botanic oe 
lead the discussion. 

Prof. R. A. Harper, Dr. Caldwell and others also took part in 
the discussion which followed. Prof. Harper introduced the 
following resolution which was adopted: 

Resolved, that the best interests of biology and of secondary 
education in New York City would be served by a conference on 
biology in New York a schools, to be held at the earliest 
possible date. 

The papers read will be elite cat in full in TORREYA. 


Meeting adjourned. 
B. O. DoncGE, 


Secretary 


105 


NEWS ITEMS 


The Board of Governors of Harvard University have appointed 
Mr. E. H. Wilson as assistant director of the Arnold Arboretum. 
Mr. Wilson returned recently from an extended exploring trip 
in the Far East. 


My mycological friends have heard much of the fungi that have 
appeared from time to time on my lawn during the past ten 
years or more. Now it is Selaginella apus that takes first place, 
having occupied during recent years an area of over 500 square 
yards, forming a soft, delicate, green carpet beneath the grass. 
It began to spread from the shaded side of the lawn, but did 
not stop spreading when it reached the sunny open spaces. By 
the middle of June, the large spore-cases are quite evident under 
a hand lens at the base of the short, crowded spikes. 

—W. A. MurRRILL. 


A testimonial dinner to Dr. N. L. Britton, director of the New 
York Botanical Garden, given by the managers at the Metro- 
politan Club on the evening of May 7, was attended by men of 
science from all parts of the country. Dr. D. T. MacDougal, 
director of the Desert Laboratory of the Carnegie Institution of 
Washington acted as toastmaster, and speeches reviewing the 
history of the organization of the garden by Dr. Britton twenty- 
three years ago, and of his widely inclusive and important re- 
searches were made by Dr. W. Gilman Thompson, president of 
the board; Professor R. A. Harper, chairman of the scientific 
directors; Professor H. F. Osborn, president of the American 
Museum of Natural History; Provost William H. Carpenter, of 
Columbia University; Dr. Arthur Hollick, director of the Staten 
Island Institute of Arts and Sciences, and Professor Geo. T. 
Moore, director of the Missouri Botanical Garden, at St. Louis. 
At the conclusion of the ceremonies Mr. Robert DeForest pre- 
sented Dr. Britton with a loving cup appropriately inscribed on 
behalf of the board of managers. Congratulatory letters and 
telegrams from distinguished scientific men were read. 


The Torrey Botanical Club 


Contributors of accepted articles and’reviews who wish six gratuitous copies 
of the number of TorreYA in which their papers appear, will kindly notify the 
editor when returning proof. 

Reprints should be ordered, when galley proof is returned to the editor. The 
' New Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
following rates: 


2pp 4pp 8pp 12pp 16pp 20pp 
25 copies $ .79 $1.14 $1.78 $2.32 $2.87 $3.28 
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100 copies 1.45 2.03 2.73 3.50 4.23 4.55 
200 copies 2.15 3.24 3.92 5 25 6.52 6.92 


Covers: 25 for $1.00, additional covers 114 cents each. 
Plates for reprints, 50 cents each per 100. 


Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs. E. G. BRITTON, Chairman. 
J. H. BARNHART, PROF. JEAN BROADHURST 
Miss.C. C. HAYNES B. O. DopGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F. J. SEAVER 
J. H. Barnuart, Chairman. Membership Committee 
R. A. HARPER ays K. SMALL, Chairman. 
N_ L. BritTon T. E. HAZEN 
A. W. Evans E. W. OLIVE 
M. A. HowE Local Flora Committee 
H. H. Russy N. L. Britton, Chairman. 
Field Committee Phanerogams: Cryptogams: 
F. W: PENNELL, Chairman. E. P. BICKNELL Mrs. E.G. Brittc x 
Mrs. L. M:. KEELER N. L. BRITTON T. B. Hazen 
MIcHAEL LEVINE C.,C. CurTIs M. A. Howe 
GEORGE T. HASTINGS K. K. MACKENZIE MICHAEL LEVINE 
Percy WILSON NORMAN TAYLOR. W. A. MuRRILL 


F. J. SEAVER 


Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M. 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F, J. Seaver 
Gasteromycetes: G.C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M:. Richards, F. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurst 


, Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


OTHER PUBLICATIONS 


OF THE 


TORREY BOTANICAL CLUB — 


£ tr) BULLETIN 
A monthly ona devoted to general botany, Re 


1870. Vol. 45 published in 1918, contained 519 pages of text) 


and 15 full-page plates. Price $4.00 per annum. For Europe, 
18 shillings. Dulau & Co., 47 Soho poate omen Are. 
agents for England, 
Of former volumes, only 24—45 can be supplied entire; cer- 
tain numbers of other volumes are available, but the entire stool 
5f some numbers has’ been reserved for the completion of sets 
Vols. 24-27 are furnished at the published price of two dollars _ 
each; Vols. 28-45 three dollars each.. As! 
Giamte copies (30 cents) will be furnished only when not 
breaking compere volumes. | 


2) MEMOIRS 


The Memoirs, established 18809, are, published, at irregu- — 
lar intervals. Volumes 1-15 are now completed; No, 1) of 
Vol. 16 has been issued. The subscription price is fixed at 
$3.00 per volume in advance; Vol. 17, containing Proceedings — 
of the Semi-Centennial Anniversary of the Club, 490 pages, was 
issued in 1918, price. $5.00. Certain numbers can also be. pur- 
chased singly. A list of titles of the individual papers ang of 

prices will be furnished on application. 


(3) The Preliminary Catalogue of Anthophyta and Pteri- 
fophyta reported as growing within one hanged miles of New 
York, 1888. | Price} $1.00. 


Correspondence relating to the above publications should be 
addressed to | 
DR. BERNARD O. DODGE 
Columbia University 


New York City’ 


Vol. 19 June, Ig9I9 No. 6 


CRI YA 


A Monruty Journar or BoranicaL Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


‘ BY 


NORMAN TAYLOR 


JOHN. TORREY, 1796-1873. 


CONTENTS 
Scrophulariaceae of the local Floral: FRANCIS W. PENNELL...+--.ese0e ceeeeeee cece es 107 
Tumion taxifolium in Georgia: ROLAND M. HARPER «..0s-tecceeseceeceseenenetenstt seers 11g 
Proceedings of the Club.......:. AN Li ee Natl BARE BS ee Re oc ee NIE 2 122 
News Items. ........... .... agi Sonat Joctoes cebls Ras Toews od ie Magia 2 ete tase a dbeaysteta scab sahe ded oaatecs 124 


PUBLISHED FOR THE CLUB 


At 41 NortH Queen Street, LANCASTER, Pa. 
BY Tue New Era Printinc Comrany 
“Entered at the Post Office at Lancaster, Pa,, as second-class matter. 


THE TORREY BOTANICAL CLUB. 


OFFICERS FOR 1019 


President 
H. M. RICHARDS, Se.D. 


Vice- Presidents. 
JOHN HENDLEY BARNHART, A.M., M.D 
C. STUART GAGER, PH.D. 


Secretary and Treasurer 
BERNARD O. DODGE, PH.D. 
CoLuMBIA UNIVERSITY, N. Y. City. 
Editor 
ALEX. W. EVANS, M.D., Px.D. 


Associate Editors 


JEAN BROADHURST, Pu.D. M.LEVINE, Pu.D. 
J. A. HARRIS, PH.D. G. E. NICHOLS, Pu.D. 


MARSHALL AVERY HOWE, Pu.D. ARLOW B. STOUT, Pu.D. 
NORMAN TAYLOR. 


Delegate to the Council of the New York Academy of Sciences 
M. A. HOWE, Px.D. 


OFFICIAL ORGAN OF THE WILD FLOWER PRESERVATION 


SociETY or AMERICA 


TorREYA is furnished to subscribers in the United States and 
Canada for one dollar per annum; single copies, fifteen cents. To 
subscribers elsewhere, five shillings, or the equivalent thereof. Postal or 
express money orders and drafts or personal checks on New York City 
banks are accepted in payment, but the rules of the New York Clearing 
House compel the request that ten cents be added to the amount of any 
other local checks that may be sent. Subscriptions are received only 
for full volumes, beginning with the January issue. Reprints will be 
furnished at cost prices. Subscriptions and remittances should be sent 
to TREASURER, TORREY BOTANICAL CLuB, 41 North Queen St., Lan- 
caster, Pa., or Columbia University, New York City. 

Matter for publication, and books and papers for review, should 
be addressed to 


NORMAN: TAYLOR 


Brooklyn Botanic Garden 
Brooklyn, N. Y 


Vr oe! 


TORREYA 


Vol. Ig No. 6 
June, IgIg 


SCROPHULARIACEAE OF THE LOCAL FLORA. I 
By Francis W. PENNELL 


In commencing the systematic study of a family of plants for 
North America there is logic in studying first those species which 
occur in the eastern seaboard of the United States. These were 
the plants first known in detail, if not necessarily those earliest 
discovered, on this continent. From Massachusetts to Carolina 
we are on classic ground, and here the plant-life has been worked 
over so many times, and each species so often collected, that 
we may now speak with certainty of nearly all specific identities. 

The present study is concerned with but a portion of this 
territory, the counties included within the local flora range, of 
the Torrey Botanical Club and of the Philadelphia Botanical 
Club. These combined include all of Connecticut; New York 
southeast of Columbia, Greene and Delaware counties inclusive; 
all of New Jersey; Pennsylvania southeast of Pike, Wayne, Lacka- 
wanna, Luzerne, Schuylkill, Lebanon, Dauphin and Lancaster 
counties inclusive; Newcastle county, Delaware; and Cecil 
county, Maryland. This area is in main part represented in 
the Torrey Club collection at the New York Botanical Garden, 
and the portion within approximately fifty miles of Philadelphia 
in the remarkably full and valuable collection of the Philadelphia 
Club at the Academy of Natural Sciences in that city. To both 
collections I have had free access, and the records below include 
data from these, the herbaria of Columbia University, the 
Brooklyn Botanic Garden, the University of Pennsylvania and 
several other institutions. To the curators of all I am appre- 
ciative. 

Nearly all the species native or naturalized within the area 


[No. 5, Vol. 19 of TORREYA, comprising pp. 85-105 was issued 9 July 1919.] 


107 


108 


of this study I have myself collected and of each made descrip- 
tions of fresh corollas, and noted other features to be gained only 
in the field. The importance of such work in taxonomic study 
needs emphasis. 

In the present revision keys are given to the genera and species. 
These are detailed for points of definite contrast. These keys 
apply only to the species of our flora, and the warning must be 
made that the generic and tribal contrasts may be of little or no 
assistance beyond this territory. But just such keys as these 
are of most value to the local worker, and moreover it is by 
combining such analyses from various regions that we may hope 
ultimately to build more thorough family keys. An inductive 
process! © 

For each genus the type-species is stated. For each native 
species information of its type is stated, quoted from the original 
describer. This includes the statement of the particular speci- 
men from which the first description was made and of the place 
of its collection. The later history of each name is traced. 
Extra-limital synonyms, even if the names have been current 
here, are not included except by brief mention. But all names 
ever proposed based upon plants occurring native in this area are 
supposed to be included. 

With respect to distribution I should like to undertake a study 
for which the data at hand in our herbaria is not yet sufficient. 
Moreover my own observations have not as yet been sufficiently 
prolonged over this area. The counties best represented in 
herbaria are those of Connecticut; New York, from the High- 
lands southeastward, including all Long Island; New Jersey, 
with considerable gaps to the northwest; Pennsylvania south- 
east of the Blue Ridge; and northern Delaware. Northwest 
of the Highlands and of the Blue Ridge botanical collections 
have been few and scattered, the regions best known being the 
Pocono Plateau of Pennsylvania, and sections of Ulster, Greene 
and Delaware counties, New York. 

Dr. Witmer Stone, in his Plants of southern New Jersey, has 
traced with a master-hand the distribution of vegetation for the 
Coastal Plain portion of that state. That regions of as sharp 


109 


delimitation occur northward and westward, through the land 
of hills, of parallel mountain-areas with intervening trough-like 
valleys, of red soil derived from Triassic rock or of black soil 
from Ordovician limestone, of various soils derived from the 
ridges of shale, gneiss and sandstone, appears self-evident. In 
the northern portion of our territory glaciers, building lake and 
gravel habitats, have left us a new series of environmental con- 
ditions. Mr. Taylor’s suggestive Flora does not attempt the 
detailed analysis of distribution which is demanded. I believe 
that the careful working-out of the ranges of the species of a 
few well-selected families of plants will give the knowledge we 
need for the dividing into phytogeographic areas of this varied 
inland—knowledge which will be nearly as definite as if multi- 
plied by such a wealth of data as is presented by Dr. Stone. 
The problem is fascinating and it is with reluctance that I realize 
that the Scrophulariaceae have not yet been observed over a 
sufficient area or with sufficient thoroughness to warrant basing 
upon this study any contribution toward such a survey. 

Our present study then attempts but these three goals: to 
present keys contrasting the genera and species of Scrophulari- 
aceae in our flora, to make certain the nomenclature, and to give 
preliminary observations of distribution. 


A. Corolla with the posterior Jobes external in the bud. 
(Antirrhinoideae.) 
B. Filaments five. Stigma capitate. Capsule septi- 
cidal. Sepals five, distinct. 
C. Corolla rotate, slightly zygomorphic, its lobes 
much longer than the tube. Filaments all with 
fertile anthers. Leaves alternate. I. VERBASCEAE. 


1. Verbascum. 
CC. Corolla tubular-campanulate, zygomorphic, its 


lobes shorter than the tube. Posterior fila- 
ment without anther, the others didynamous. 
Leaves opposite. II. CHELONEAE. 
Corolla white, lavender or pink, pubescent or 
puberulent within, its anterior lobes pro- 
jecting. Sterile filament slender, filiform, 
white. 
Corolla membranous, white or lavender, 
puberulent or somewhat pubescent within 
over base of anterior lobes. Sterile fila- 


110 


ment as long as the others, pubescent on 
its posterior face. Anther-sacs distinct, 
glabrous or barbate with short hairs. 
Sepals lanceolate to ovate, acute to acumi- 
nate. Seedswingless. Inflorescence com- 
pound, a raceme of cymosely branching lax 
flower-clusters. Stem-leaves clasping. 2. Penstemon. 
Corolla semi-fleshy, white or rose, densely 
pubescent within over base of anterior 
lobes. Sterile filament much shorter than 
others, glabrous. Anther-sacs becoming 
confluent, densely lanose. Sepals ovate- 
orbicular, rounded. Seeds winged. In- 
florescence simple, a spike-like raceme of 
single flowers on short - several-bracted 
pedicels. Stem-leaves narrowed at base, 
short-petioled. 3. Chelone. 
Corolla red-brown, glabrous within, its antero- 
lateral lobes vertically projecting, the anterior 
lobe deflexed. Sterile filament shorter than 
wide, two-lobed, yellow or red-brown. In- 
florescence compound. - 4. Scrophularia. 
BB. Filaments four or two, the posterior one being lost. 
C. Acaulescent. Corolla rotate, slightly zygo- 
morphic, white or lavender-tinged. Capsule two- 
celled at base, septicidal. Stigmacapitate. Small 
herb, spreading by stolons. III. LIMOSELLEAE. 
5. Limosella. 
CC. Caulescent, with leaves mainly cauline. Corolla 
zygomorphic, the lobes shorter than the tube. 
Capsule two-celled throughout. Inflorescence 
simpiy racemose. 
D. Leaves opposite. Corolla without a spur. 
Stigma of two usually plate-like lobes. 
Capsule septicidal, or somewhat loculicidal 
by a simple split down median line of 
carpel. IV. GRATIOLEAE. 
Corolla yellow or white, with throat four- 
angled, its orifice open; pubescent within 
at base of posterior lobes. Postero-lateral 
stamens perfect, antero-lateral reduced to 
sterile filaments or wanting. Several 
bractlets at base of the five distinct sepals. 
Capsule septicidal, or tardily slightly 
loculicidal. 6. Gratiola. 
Corolla yellow or lavender-blue, with throat 
somewhat flattened into a horizontal 
plane, channeled beneath and arched 


Eh 


posteriorly; pubescent within at base 
of anterior lobes. No bractlets below 
calyx. 

Perfect stamens four, with slender straight 
filaments. Corolla 15-30 mm. long, 
its orifice nearly closed by the raised 
anterior lip; the posterior lobes round- 
ed and nearly equaling anterior. Style 
without tubercle-like base. Capsule 
loculicidal, tardily somewhat septicidal. 
Sepals united over one-half length. 

Perfect stamens two; the antero-lateral 

filaments fused with corolla ridges, 
from near apex of which abruptly 
upcurving. Corolla lavender, 2-10 
mm. long, its orifice open; the pos- 
terior lobes acute and shorter than 
the anterior, or else wanting. Style 
with white persistent tubercle-like 
base. Capsule septicidal, the thin 
plate-like septum persisting. 

Corolla 6—10 mm. long, with two pos- 
terior lobes developed. Postero- 
lateral stamens perfect, antero- 
lateral filaments without anthers. 
Sepals five, united at base. Plants 
erect or ascending, with leaves I-3 
cm. long. 

Corolla 2 mm. long, with two posterior 
lobes lost. Postero-lateral stamens 
lost, antero-lateral filaments with 
anthers. Sepals four (the posterior 
lost), united nearly four fifths their 
length. Plant repent, with leaves 
.3--5 cm. long. 

DD. Leaves alternate. Corolla with a spur at 
the base of the anterior petal. Stigma capi- 
tate. Capsule loculicidal, the septum with 
adjacent capsule-wall persisting, the remaining 
wall splitting irregularly. 


AA. Corolla with the anterior lobes external in the bud. 
(Rhinanthoideae.) 

B. Stamens two, the postero-laterals present, the 
antero-laterals completely lost. Antero-lateral 
lobes of corolla external in bud. Not parasitic. 
Sepals four, the posterior lost. Posterior lobes of 
corolla completely fused. 


7 


Io. 


Wile 


Mimulus- 


. Ilysanthes- 


Hemianthus. 


ANTIRRHINEAE- 
Linaria. 


DIGITALEAE. 


12 


Leaves whorled. Corolla white, its lobes shorter 
than thetube. Capsule acute, longer than broad, 
not flattened. Plant 10-20 dm. tall. It. Veronicastrum. 
Leaves opposite oralternate. Corolla blue, its lobes 
longer than the tube. Capsule acute to deeply 
notched, broader than long, flattened. Plants 
lower. 12. Veronica. 
BB. Stamens four, didynamous, the antero-laterals 
usually slightly the longer. Parasitic on roots of 
other plants. 
C. Sepals five, alike, more or less united. Corolla- 
lobes all somewhat distinct, the posterior 
spreading or broadly arched; anterior lobe 
external inbud. Stigmaelongated. Capsule 
loculicidal, splitting through septum. VII. BUCHNEREAE. 
Corolla yellow or pink, campanulate, with in- 
flated throat and open orifice. Stamens 
all perfect, the anthers two-celled, lanose. 
Two stigmatic lines down each side of 
style-apex. Filaments and style nearly 
as long as the tube of the corolla. Capsule 
exserted from the calyx-tube. 
Corolla yellow. Capsule acute to acumi- 
nate. Leaves lanceolate to ovate, entire 
to bipinnatifid, petioled. Stem stout, 
over 4 dm. tall. Perennials or annuals. 13. Aureolaria. 
Corolla pink, with red spots within on an- 
terior side. Capsule rounded, with a 
mucro. Leaves filiform to lanceolate, 
entire or auriculate-lobed at base, 
sessile. Stem slender, usually lower. 
Annuals. 
Stem ascending-scabrellous to’ glabrous. 
Leaves linear to filiform, entire. Pedi- 
cels over I mm. long. +Calyx-lobes 
linear to subulate, slightly longer to 
usually much shorter than the tube. 
Corolla with two yellow lines within 
throat anteriorly. Anther-sacs of both 
pairs of stamens uniform. Capsule 
globose to globose-ovoid, 3—7 mm. long. 
Seeds closely reticulate. 14. Agalinis. 
Stem retrorse-hispid. Leaves lanceolate, 
usually auriculate-lobed at base. Pedi- 
cels less than 1 mm. long. Calyx- 
lobes ovate, longer than the tube. 
Corolla without yellow lines within 
throat anteriorly. Anther-sacs of pos- 


113 


terior pair of stamens shorter. Cap- 
sule broadly ovate, 10-13 mm. long. 
Seeds reticulate with raised ridges. 15. Olophylla. ~-" 
Corolla purple-blue, salverform, the tube very 
narrow and densely pilose, the lobes widely 
spreading. Postero-lateral stamens becom- 
ing rudimentary, the antero-laterals with but 
one anther-sac. Stigmatic area over entire 
surface of style apex. Filaments and style 
less than one half length of corolla-tube. 
Capsule equaled by and enclosed within calyx- 
tube. 16. Buchnera, 
CC. Posterior sepal shorter or wanting. Corolla 
decidedly two-lipped, the posterior lobes united 
and arched nearly to apex, the anterior lobes 
usually shorter; anterior or one antero-lateral 
lobes external in bud. Stigma short, capi- 
tate. VIII. RHINANTHEAE, 
Posterior sepal shorter than others. Capsule 
turgid, septicidal, only tardily slightly loculi- 
cidal. Seeds linear, flat, 2 mm. long. 17. Schwalbea. 
Posterior sepal wanting. Capsule flattened, 
loculicidal, splitting through septum. 
Corolla with posterior lobes projecting, not 
hooded at apex, the anterior lobes very 
short, thickened, deep-green. Seeds many, 
reticulate. Bracts foliaceous, distally 
scarlet. 18. Castilleja. 
Corolla with posterior lobes arched, hooded 
at apex, the anterior lobes membranous, 
flat, colored. Seeds few, not reticulate. 
Bracts not colored. 
Corolla yellow or pink throughout, the 
anterior lip not raised into a palate. 
Seeds more than two. Sepals of 
each side united nearly or quite to 
apex. Leaves crenate-serrate to 
bipinnatifid-lobed. 
Corolla1z2mm.long. Anthers lanose. 
Capsule circular, equally two- 
celled, splitting on both posterior 
and anterior sides. Seeds 5 mm. 
long, circular, flat, broadly winged. 
Sepals as long as the capsule, on 
each side united nearly to apex. 
Leaves crenate-serrate. Annual. 19. Rhinanthus. 
Corolla 15-20 mm. long. Anthers 
giabrous. Capsule ensiform, un- 


s 114 


equally two-celled, splitting only on 
posterior side. Seeds r mm. long, 
oblong, cylindric, not winged. Sep- 
als less than one half length of 
capsule, on each side united to 
apex. Leaves bipinnatifid-lobed. 


Perennials. 20. Pedicularis. 


Corolla white, the anterior lip raised into 
a yellow densely pubescent palate. 
Seeds maturing two to a capsule. 
Sepals united at base only, the two 
postero-laterals longer. Leaves lance- 
olate, entire or setaceous-toothed near 


base. 21. Melampyrum. 


TeVERBASCUM Li: Spy Pla77. bss 


Type species, V. Thapsus L. of Europe. - 


Leaves glabrous. Stem above and calyx with simple glandular 
hairs. Corolla yellow or white. Filaments all densely lanose 
with knobbed purple hairs. Pedicels 10-15 mm.long. Cap- 
sule subglobose, glandular-puberulent. Seeds .8—.9 mm. 
long, dark-gray. 

Leaves, stem and calyx more or less pubescent with stellately- 
branched non-glandular hairs. Corollas always yellow. 
Filaments: three posterior lanose, two anterior sparingly 
lanose to glabrous, with filiiorm yellow hairs. Pedicels 
less than 10 mm.long. Capsules ovoid or oblong, stellate- 
pubescent. Seeds .4—.7 mm. long, brownish-gray. 

Leaves dark and becoming glabrate above, whitened be- 

neath, sessile or the lower petiolate, not decurrent. Pedi- 
‘cels reaching 10 mm. long, clustered three to twelve in an 
axil. Sepals linear, 2-2.5 mm. long, much shorter than 
the mature capsule. Corolla 18 mm. wide. Capsule 4 
mm. long. Seeds 6-7 mm. long. 

Leaves dull- or yellowish-green and permanently pubescent 
above, scarcely paler beneath, sessile, more or less 
decurrent. Pedicels reaching 5 mm. long, one to five 
inanaxil. Sepals ovate, 6-8 mm. long, slightly shorter 
than to equaling the mature capsule. Corolla 20-35 
mm. wide. Capsule 6-8 mm. long. Seeds .4—.5 mm. 
long. 

Stem-leaves broadly ovate, strongly crenate, dull-green, 
moderately pubescent. Pedicels reaching 5 mm. long, 
three to five to an axil. Inflorescence interrupted. 
Corolla 30-35 mm. wide. 


HH 


. V. Blattaria. 


2. V. Lychnitis. 


3- 


V. phlomoides. 


115 


Stem-leaves lanceolate, finely crenate, yellowish-green, 


very densely pubescent. Inflorescence crowded. 7 
Pedicels very short to none, one to an axil. Corolla 
20-22 mm. wide. 4. V. Thapsus. 


I. VERBASCUM BLATTARIA L., 

Flowering from mid-June to mid-August, fruiting from early 
July on. 

Loam soil, cultivated fields, common throughout the area 
above the Fall-line, rarely recorded from the Coastal Plain. 
Naturalized from Eurasia. 


2. VERBASCUM LYCHNITIS L. 
Flowering from late June to August, fruiting from August on. 
Loam soil, roadsides, local in the area above the Fall-line, 
especially near the cities. Naturalized from Eurasia. 


3. VERBASCUM PHLOMOIDES L. 

Collected in flower in July and August. 

Probably sandy soil, cultivated fields; rare. Garden City, 
L. I.; Lindenwold, N. J. Adventitive from Eurasia. 


4. VERBASCUM THAPSUS L. 

Flowering from mid-July to late oar fruiting in August 
and September. 

Mainly in loam soil, fields and roadsides; common throughout, 
mainly above the Fall-line. Naturalized from Eurasia. 


2. PENSTEMON [Mitchell Schmidel, Icones Plantarum 2. 1762 


Type species, Chelone Penstemon L., ‘‘ Habitat in Virginia.”’ 


Corolla funnelform; throat tubular; lobes widely spreading; 
puberulent within. Leaves entire or the upper slightly 
serrulate, glabrous, under a lens evidently puncticulate. 
Seeds strongly ridge-angled. 1. P. tubiflorus. 

Corolla with throat tubular near base, then abruptly inflated; 

pubescent within at base of anterior lobes. Leaves more 
or less denticulate, not evidently puncticulate under a 
lens. Seeds not strongly ridge-angled. 

Corolla with throat inflated, its mouth open, not closed by 
the anterior lip. Sterile filament slightly to moder- 
ately densely bearded. Calyx-lobes ovate-lanceolate 
to lanceolate. Plants taller, glabrous to puberulent. 


116 


Corolla white, rather strongly inflated. Anther-sacs 


usually barbate. Stem glabrous or nearly so. 2. P. Digitalis. 
Corolla light violet-purple, moderately inflated. Anther- 
sacs glabrous. Stem puberulent. 3. P. Pentstemon. 


Corolla with throat scarcely inflated, its mouth closed by the 
anterior lip, which closes as a convex arc. Sterile fila- 
ment very densely bearded. Calyx-lobes ovate. 
Plants lower, the stem pubescent or hirsute. 
Corolla 15-20 mm. long, white with violet lines. Anther- 
sacs oval. Calyx-lobes obtuse to short-acuminate. 
Stem and leaves soft-canescent. Leaves lanceolate. 4. P. pallidus. 
Corolla 23-28 mm. long, lavender-purple, unlined. An- 
ther-sacs triangular-orbicular. Calyx-lobes acumi- 
nate to caudate. Stem and frequently midrib of 
leaves beneath more or less lanose-hirsute. Leaves 
lanceolate-attenuate. 5. P. hirsutus. 


I. PENSTEMON TUBIFLORUS Nutt. 

Flowering in June. 

Fields, seen only from Spring Valley, Rockland Co., N. Y. 
Introduced from the southwestern Mississippi Valley. 


2. PENSTEMON DIGITALIS Nutt. 

Flowering from mid-June to early July, fruiting in late August 
and September. 

Fields and meadows, frequent above Fall-line. Introduced 
from the southwestern Mississippi Valley. 


3. PENSTEMON PENTSTEMON (L.) MacMiuillan. 

Flowering in June and July. 

Fields and meadows, seen only from- Rockland Co., New York 
and Bergen and Gloucester counties, New Jersey. Introduced 
from the South Atlantic states. 

4. PENSTEMON PALLIDUS Small, Fl. S. E. Un. St. 1060, 1337. 
1903. 
“Type, Bedford, N. Y., Britton, June, 1900, in Herb. N. Y. 
B. G.”’ Type seen; also the plant re-collected and 
studied at the type-station. 

Flowering from mid-May to late June. 

Sandy or barren soil, occasional, mostly above the Fall-Line. 
Certainly introduced from the central Mississippi Valley. 


5. PENSTEMON HIRSUTUS (L.) Willd. 
Chelone hirsuta 1., Sp. Pl. 611. 1753.. Habitat ivi 


t17 


ginia.”” Based upon Clayton n. 39 in the Gronovian 
Herbarium. The Linnean characterization certainly de- 
notes the plant here considered. 

Penstemon hirsutus (L.) Willd., Sp. Pl. 3: 227. 1800. 
Flowering from late May to early July, fruiting from July on. 
Dry fields, usually sandy, in potassic soil, occasional or local 

through the area above the Fall-line. Ranges from southern 
Vermont and southern Ontario to upland Virginia, Kentucky and 
southern Michigan.* 


3. CHELONE L., Sp. PI. 611. 1753 
Type species, C. glabra L. 


tI. CHELONE GLABRA L., Sp. Pl. 611. 1753. “Habitat in Vir- 


ginia, Canada.’’ Based upon a plant grown in the Clif- 
ford garden in Holland. 

Chlonanthes tomentosa Raf., New Fl. Am. 2:20. 1837. “In 
the mts. of Virginia.” Leaves tomentose or pubescent 
beneath; a condition of more frequent occurrence south- 
ward, specimens noted from Monmouth, Burlington and 
Camden counties, New Jersey, and frequently through 
southeastern Pennsylvania. Here treated as a form, 
tomentosa (Raf.) Pennell, forma nova. 

Flowering from early August to early October, fruiting from 
mid-September on. 

Moist loam to sandy woodland, in potassic soil, frequent to 
common throughout above the Fall-line; frequent or occasional 
through the Coastal Plain, outside of the Pine Barrens. The 
leaves tend to be narrower in the Coastal Plain. Ranges from 
Newfoundland to Manitoba, northern Florida and Kansas. 


4. SCROPHULARIA L., Sp. Pl. 619. 1753: 


Type species, S. nodosa L., “‘ Habitat in Europae succulentes.”’ 


Petioles stouter, evidently wing-margined. Leaves cuneate 
to truncate at base, coarsely serrate to dentate. Inflores- 
cence narrowly elongate, 4-8 cm. wide, its branches rela- 


* PAULOWNIA TOMENTOSA (Thunb.) Baill. 
A tree with lavender flowers, is an occasional escape from cultivation to road- 
sides, railroad-banks and thickets. Adventive from eastern Asia. 


118 


tively stout. Calyx-lobes triangular-obtuse. Corolla 8-12 

mm. long. Fertile filaments more evidently pulverulent. 

Sterile filament 1.8 mm. wide, yellow. Capsule pyramidal- 

acuminate, 5-10 mm. long. Seeds .8—-1 mm. long, reticu- 

late with transverse areas. Flowering in early summer. 1. S. leporella. 
Petioles slender, scarcely margined. Leaves narrowed to cord- 

ate at base, more finely crenate-serrate. Inflorescence pyra- 

midal, 5-18 cm. wide, its branches slender. Calyx-lobes 

more broadly rounded. Corolla 6-8 mm. long. Fertile 

filaments very finely pulverulent. Sterile filament 1 mm. 

wide, purple-brown. Capsule ovoid, acute, 4-7 mm. long. 

Seeds .5-.8 mm. long, plump, reticulate with more nearly 

hexagonal areas. Flowering in late summer. 2. S. marilandica. 


SCROPHULARIA LEPORELLA Bickn. in Bull. Torr. Bot. Club 23: 


317. 1896. ‘‘Common near New York City. . . . I have 
met with it within eight miles of the Connecticut line and in 
the Pocono region of eastern Pennsylvania.” Specimen 


from Bronxville, Westchester Co., New York, collected 
by E. P. Bicknell June 15, 1895, seen in herbarium Colum- 
bia University at The New York Botanical Garden. 

Only inconstantly to be distinguished from S. occidentalis 
(Rydb.) Bicknell of the Rocky Mountain and High Plains states 
by its leaves being less coarsely and more evenly serrate (in 
occidentalis frequently coarsely toothed at base), and the branches 
of the inflorescence being usually less stowit and less densely 
glandular. Probably better considered as a geographic variety. 

Flowering from mid-May to mid-July, fruiting from late June 
to late August. 

Meadows and thickets, loam, in potassic soil, frequent through- 
out above the Fall-line; less frequent or occasional on Long 
Island, and in the Middle and Cape May district of New Jersey. 
Ranges from Quebec to Connecticut and Virginia, westward to 
North Dakota and Nebraska where it appears to pass into S. 
occidentalis. 


2. SCROPHULARIA MARILANDICA L., Sp. Pl. 619. 1753. ‘‘Habi- 
tat in Virginia.’ Linné had no specimen in his her- 
barium in 1753, but his description is copied from Hortus 
Upsalensis 177. 1748. From the diagnosis there given, 
especially the mention of leaves cordate serrate, and of 


119 


petiole but very slightly decurrent, the plant of the 
Upsala Garden would appear to have been the species 
now considered. 

Scrophularia lanceolata Pursh, Fl. Am. Sept. 2: 419. 1814. 
“In wet meadows and woods: Pennsylvania.’’ Descrip- 
tion apparently of this. The type of this should be veri- 
fied, but the description of the petioles as not ciliate, and 
the lateness of the time of flowering would indicate that 
Pursh described as new the original marilandica. 

Scrophularia nodosa marilandica (L.) A. Gray, Syn. Fl. N. 
Am, 2.1: 258. 1878. 

Scrophularia nodosa lanceolata (Pursh) M. E. Jones, Contrib. 
West. Bot. 12:67. 1908. 

Flowering from late July to late September, fruiting from 
early August into October. 

Open woodland, loam, in potassic soil, frequent or northward 
rare through the area above the Fall-line; occasional in western 
Long Island, and near the Delaware River in the Middle District 
of New Jersey. Ranges from Massachusetts and southern On- 
tario to Georgia, Arkansas and Nebraska. 


(To be continued.) 


TUMION TAXIFOLIUM IN GEORGIA 


By RoOLanp M. HARPER 


The Florida “savin” or “stinking cedar,” Tumion taxifolium 
(Arn.) Greene (Torreya taxifolia Arn.) an evergreen tree closely 
related to the yews, ever since its discovery by H. B. Croom 
near Aspalaga in western Middle Florida about 85 years ago, 
has been celebrated in botanical circles on account of its very 
restricted distribution and its belonging to a genus which was 
widespread in pre-historic times but is now practically confined 
to Florida, California, China and Japan.* 


* Existing knowledge about this tree is pretty well summed up in the following 
works: Asa Gray, Am. Agriculturist 34: 266-267. 1875 (reprinted with some 
alterations in ‘‘Scientific Papers of Asa Gray,” 1: 188-196. 1889); A. H. Curtiss, 
Tenth Census U. S, 9: 521. 1884; A. W. Chapman, Bot. Gaz. 10: 251-254. 
1885; G. V. Nash, Bull. Torrey Club 23: 96. 1896; H. C. Cowles, Rep. 8th 


120 


For many years previous to the time herein noted it was known 
only on the east side of the Apalachicola River in Gadsden and 
Liberty Counties, Florida, from Chattahoochee to Alum Bluff, 
a distance of about twenty miles. (There have been unverified 
rumors of its occurrence away from the river in Jackson and 
Wakulla Counties.) Its usual habitat is shaded bluffs and 
ravines, in the neighborhood of outcrops of the Chattahoochee 
formation (an argillaceous limestone), and most of it is close 
to the river, though some specimens have been seen a mile or 
two up the valleys of tributary creeks. The locality oftenest 
visited is near River Junction, a small place near the northern 
edge of the state, which has had one railroad for over forty years, 
and four for the last twelve years. On account of the restricted 
range of the tree, some writers have imagined it to be on the 
verge of extinction; but it is quite abundant yet, especially in 
the vicinity of Aspalaga, where it was first discovered, and it 
does not seem to be in any immediate danger. (Its near relative 
Taxus Floridana, curiously enough, grows in the same region 
and is much rarer, but somehow it has attracted very little 
attention among botanists. The Tumion may have achieved 
notoriety mainly through being named first for Dr. Torrey, and 
having been made the object of a pilgrimage by Dr. Gray in 
the days when it bore the name of Torreya.) 

In August, 1903, while botanizing in extreme southwestern 
Georgia, I remembered that this famous tree grew within a mile 
or two of the Georgia line, and thought it would be a simple 
matter to find it on the Georgia side, a matter which no one 
apparently had made any special effort to do. So I went one 
day to River Junction and had a native guide me to the nearest 
colony of the tree, and after taking a good look at it I spent nearly 
two days walking up along and near the river to Bainbridge; 
but I saw no Tumion outside of the colony first shown to me. 
In the light of subsequent developments it is now evident that 
after crossing the state line I stayed in the alluvial bottoms of 
the river too long, and did not turn out into the bluffs until I 


Int. Geog. Cong. 599. 1905; Sellards & Gunter, Ann. Rep. Fla. Geol. Surv. 2: 
262. 1910; R. M. Harper, Bull. Torrey Club 32: 149. 1905; Torreya 11: 225—- 
226. 1911; Ann. Rep. Fla. Geol. Surv. 6: 212, 215, 354, 41I, 412. I914. 


121 


had passed beyond the northern limit of the tree, perhaps a mile 
or two from the line. No detailed maps of the neighborhood . 
were available then (or now), which made it difficult to get my 
bearings. 

The imaginary line which forms the greater part of the bound- 
ary between Georgia and Florida is supposed to take the most 
direct course from the confluence of the Flint and Chattahoochee 
Rivers to the head of the St. Mary’s, bearing about S. 87° E.; 
but surveying a straight line to connect two points over 150 
miles apart involves serious engineering difficulties, and three 
lines were run at different times in the last century, varying a 
mile or so near the middle. The northernmost was finally 
selected as the boundary, but at the point under consideration, 
about a mile from the western extremity of the line, the possible 
error is only a few yards. 

While working in Florida between 1908 and 1915 I visited 
River Junction a few times, and saw the Tumion near there, but 
made no further effort to determine its northern limit. But 
on August 16, 1918, while on business for the U. S. Bureau of 
Plant Industry, I had a few hours between trains there, during 
which I explored the neighborhood a little, not having been 
there at that season since 1903. 

The northern boundary of the grounds of the Florida Insane 
Hospital at Chattahoochee, about a mile and a half north of 
River Junction, is marked by a stout wire fence which is said 
to be exactly on the state line, and terminates on the west about a 
mile from the river, at a road running approximately north and 
south. Having followed the boundary fence until I came to 
the road, I turned north into {Ceorgia, and about a hundred 
yards farther on, seeing some interesting-looking woods at the 
left of the road, I entered them. A few steps down the slope, 
a ravine appeared at my right (i.e., north), and in that I found 
several trees of Tumion taxifolium, some about a foot in diameter 
and forty feet tall, together with its common associates, Magnolia 
grandiflora, Fagus, Liriodendron, Ilex opaca, Acer Floridanum, 
Pinus glabra, Quercus alba, Pinus Taeda, Cercis, Ostrya and 
Liquidambar (to mention trees only). 


122 


The mere extension of the known range of this tree northward 
about a mile would hardly be worth mentioning, but for the fact 
that the species has been written about so much, and the new 
locality being in a different state will necessitate a modification 
of the statements about it in books about North American trees, 
Georgia plants, etc. The present indications are that it does 
not extend into Georgia more than a mile. A few specimens 
were collected and afterwards distributed to the leading Ameri- 
can herbaria, for the benefit of persons who may attach more 
importance to the possibility of identifying the species (even 
such an unmistakable one as this) wrongly than to that of making 
a false or erroneous or inadequate statement on the label about 
the locality. (In other words, there are probably some tax- 
onomists who if no specimens existed to back it would not take 
cognizance of this report of a new locality, but seeing a specimen 
labeled Georgia in large type would not worry about the possi- 
bility of a slight error in latitude.) 


UNIVERSITY, ALA. 


PROCEEDINGS OF THE CLUB 
MARCH 25, 1919 

The second meeting for March was a special evening meeting 
held in the Laboratory Building of the Brooklyn Botanic Garden, 
Tuesday, March 25, under the joint auspices of the Club and 
Garden. Vice-president Gager called the meeting to order at 
8:25 P.M. There were 53 persons present. No business was 
transacted. 

The program consisted of a series of motion pictures on plant 
life shown by courtesy of the U. S. Department of Agriculture, 
whose representative, Dr. R. B. Harvey, of the Bureau of Plant 
Industry, Plant Physiology and Fermentation Investigations, 
gave the lecture. 

The first film showed a series of views of various operations 
performed in connection with strawberry culture in Kentucky, 
cultivating, hoeing, inspecting, picking, sorting, packing, load- 
ing, refrigerating and consuming were among the operations 
depicted. 


125 


The second picture showed the movement of the protoplasm 
in the cells of a leaf of Elodea. Another view showed the flow . 
of protoplasm in the hypha of the fungus Pythiwm. 

Dr. Harvey then spoke of the disease of potatoes known as 
leak caused by the parasite Pythium which is doing so much 
damage in the potato region of San Juaquin Valley in California. 
The speaker explained in considerable detail how the pictures 
were obtained. The pictures showed the behavior of a hypha 
during the act of penetrating the wall of a cell of the potato 
tuber. 

Informal discussion followed the lecture. Meeting adjourned. 

B. O. DonceE, 
Secretary 
APRIL 8, I919 

The first meeting in April was held at the American Museum 
of Natural History. President Richards called the meeting to 
order at 8:15 P.M. There were 25 persons present. 

As there was no business to be transacted, the reading of 
minutes was postponed. 

Dr. J. N. Rose, National Museum, Washington, D. C., gave 
an illustrated lecture on Botanical Explorations in Equador. 
The following abstract was prepared by the speaker: 

“Dr. Rose gave an account of his recent botanical trip to 
Ecuador where he went in 1918 to inaugurate the codperative 
investigation of the flora of South America which has recently 
been organized by the United States National Museum, The 
New York Botanical Garden and the Gray Herbarium of Harvard 
University. 

“He described in some detail the flora which is seen in going 
from Guayaquil on the coast to the high Andean Valley. He also 
described his trip to southern Ecuador, where he traveled over 
the old route followed by Humboldt and Bonpland more than a 
hundred years before. On this expedition he re-collected many 
of the species obtained previously by Humboldt, collecting some 
of them from the exact locality from which they had been 
reported by him. 

“His chief work was done about the little town of Huigra, 


124 


situated at an altitude of 4,000 feet, which he found a most 
convenient base from which to make excursions. 

“Dr. Rose also told of his trip across southern Ecuador from 
Loja to the coast when he collected a number of very interesting 
cactus types of which quite a number were new to science. 

‘““Among the plants which were especially interesting were a 
species of Juglans similar to the black walnut of the United 
States, several mountain species of Carica, a species of Zamia, 
various Cinchona species, four or five species of Brugmansia, 
some of which deserve cultivation as ornamentals, a striking 
species of Gunnera, several species of Tropaeolum and various 
species of Rubus and Berberis. - He collected about two thousand 
numbers of plants.”’ 

Adjournment followed. 

B. O. DoDGE, 


Secretary 
NEWS ITEMS 


Oliver A. Farwell, instructor in botany in the Detroit College 
of Pharmacy has been appointed Professor of botany and 
phamacognosy vice Walter H. Blome, M.S., Ph.C., professor of 
materia medica and pharmacognosy, resigned. 


Dr. B. M. Duggar, of the Missouri Botanical Garden, is 
spending the summer at the Coastal Laboratory of the Car- 
negie Institution, Carmel, Cal., engaged in a continuation of 
his work on hydrogen ion concentration in plant cultures. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of Torreya in which their papers appear, will kindly notify the 
editor when returning proof. 

Reprints should be ordered, when galley proof is returned to the editor. The 
New Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
following rates: 


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Covers: 25 for $1.00, additional covers 114 cents each. 
Plates for reprints, 50 cents each per 100. 


Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs. E. G. Britton, Chairman. 
J. H. BARNHART, Pror. JEAN BROADHURST 
Miss C. C. HAYNES B. O. DoDGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F. J. SEAVER 
J. H. BaRNnwarRT, Chairman. Membership Committee 
R. A. HARPER J. K. SMALL, Chairman. 
N. L. BRITTON T. E. HAZEN 
A. W. Evans E. W. OLIVE 
M. A. Howe Local Flora Committee 
H. H. Russy N. L. Britton, Chairman. 
Field Committee Phanerogams: Cryptogams: 
F. W. PENNELL, Chairman. E. P. BICKNELL Mrs. E.G. BRITTON 
Mrs, L. M. KEELER N. L. BRITTON T. E. HAazEn 
MICHAEL LEVINE C. C. CurTIS M. A. Howe 
GEORGE T. HASTINGS K. K. MACKENZIE MICHAEL LEVINE 
PErcy WILSON NORMAN TAYLOR W. A. MuRRILL 


F. J. SEAVER 


Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M. Richards, F. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurst 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


OTHER PUBLICATIONS 


OF THE 


TORREY BOTANICAL CLUB ~ 


(1) BULLETIN 


A monthly journal devoted to general botany, established 
1870. Vol. 45 published in 1918, contained 519 pages of text 
and 15 full-page plates. Price $4.00 per annum: For Europe, - 
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Of former volumes, only 24—45 can be supplied entire : cer- 
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Vols. 24-27 are furnished at the published price of two dollars 
each; Vols. 28-45 three dollars each. 

Shae copies (30 cents) will be furnished ee when not 
breaking complete volumes. 


(2) MEMOIRS 


The Memnorrs, established 1889, are published at rer 
lar intervals. Volumes I-15 are now completed ; No. 1 of 
Vol. 16 has been issued. The subscription price is aaa at 
$3.00 per volume in advance ;. Vol. 17, containing Proceedings 
of the Semi-Centennial Anniversary of the Club, 490 pages,.was 
issued in 1918, price $5.00. Certain numbers can also be pur- 
chased singly. A list of titles of the individual papers and of © 
prices will be furnished on application. 


(3) The Preliminary Catalogue of Anthophyta and Pteri- 
dophyta reported as growing within one hundred miles of New 
York, 1888. Price, $1.00. 


Correspondence relating to the above publications should be 
addressed to 
DR. BERNARD O, DODGE 
Columbia University 


New York City 


Vol. 19 July, Ig9I9 No. 7 


TORRE YA: 


A Montuty Journat or Boranicat Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873. 


CONTENTS 
The Sedges of the Lake George Flora: SrEwarT H. BURNHAM....---.200+cseees -eeceees 125 
Some Western Columbines: T. D. A. COCKERELL.«.......seccsseeenseserrastensetesnvtnireees 137 
Shorter Notes: 
Rhamnus dahurica in Michigan: H. A. GLEASON-..++.:ccseesteecrteeseseeeeeecrecerees 141 
PERO RLOMIS SS coe ck ncn eens dE g Masts oe teed fue U de drteie POUR ab aE ss gag o Unne tot grep sbdeps to due raven 142 


PUBLISHED FOR THE CLUB 


AT 41 NortH Queen Srreet, LANCASTER, Pa. 
sy Tue New Era Printing Comrany 
“Entered at the Post Office at Lancaster, Pa,., as second-class matter, 


THE TORREY BOTANICAL CLUB 


OFFICERS FOR 10919 


President 
H. M. RICHARDS, Sc.D. 


Vice Presidents. 
JOHN HENDLEY 'BARNHART, A.M., M.D 
-C. STUART GAGER, Pu.D. 


Secretary and Treasurer 
BERNARD O. DODGE, PH.D. 
COLUMBIA UNIVERSITY, N.« Y. City. 
Editor 
ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


JEAN BROADHURST, Pu.D. M. LEVINE, Pu.D. 
J. A. HARRIS, Pu.D. G. E. NICHOLS, Pu.D. 
MARSHALL AVERY HOWE, Pu.D. ARLOW B. STOUT, PH.D. 


, NORMAN TAYLOR. f 


Delegate to the Council of the New York Academy of Sciences 
M. A. HOWE, PH.D. 


OFFICIAL ORGAN OF THE WILD FLOWER PRESERVATION 
SocIETY OF AMERICA 


Torreya is furnished to subscribers in the United States and 
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Matter for publication, and books and papers for review, should 
be addressed to 


NORMAN TAYLOR 


Brooklyn Botanic Garden 
Brooklyn, N. Y¥ 


1919 


SEP 15 


TORREYA 


Vol. I9 No. 7 
July, 1919 


THE SEDGES OF THE LAKE GEORGE FLORA 


By STEWART H. BURNHAM 


The collection and study of the Cyperaceae was begun in 
1891. It was Dr. Alvan Wentworth Chapman who awakened 
my interest in carices: and who named and verified my earlier 
collections, March 11, 1892 and January 18, 1893. In Gray 
Memorial Botanical Chapter of the Agassiz Association Bull. 
I: 7-8. 1893, there is a list of sixty-five ‘“‘Carices”’ of Vaughns 
and vicinity, compiled March 29, 1893. In this list Carex aperta, 
C. Oederi and C. squarrosa should be eliminated. 

The region covered by the Flora includes the counties of 
Washington, Warren and Saratoga. There are a few additional 
records from Mt. Defiance, Ticonderoga, Essex County. Dr. 
E. A. Burt collected carices about East Galway, Saratoga County, 
about 1880: these are preserved in his herbarium and have been 
verified by Dr. Ezra Brainerd. Mr. Frank Dobbin has collected 
many sedges near Shushan and Cambridge in southern Washing- 
ton county, specially from 1903 to 1911. Dr. Chas. H. Hall 
collected sedges in 1880 at Lake George, probably near Bolton: 
these are preserved in the Herbarium of the Brooklyn Botanic 
Garden. Dr. E. C. Howe collected about Fort Edward and in 
Hartford, from 1863’ to 1866: and some of these specimens are 


presumably preserved in the N. Y. State Herbarium and in the 


Herbarium of the N. Y. Botanical Garden. Dr. Smith Ely 
Jelliffe collected sedges about Huletts Landing, Lake George, 
in 1887-1888: these may be found in his herbarium in New 
York City. Dr. Chas..H. Peck also collected many sedges in 
the territory; which are preserved in the N. Y. State Herbarium. 

There are many sedges, particularly carices, that have not 


[No. 6, Vol. 19 of ToRREYA, comprising pp. 107-124, was issued 7 August, 1919] 


125 


Yf\ 


126 


been recorded for the Lake George region that undoubtedly 
occur there. A careful survey of the higher mountains in the 
vicinity of North Creek, Warren county would. probably add 
some additional species to the following list. 


LIsT OF SPEC:ES 


Cyperus diandrus Torr. Wet places and about ponds; not com- 
mon. Providence (E. A. Burt); Mud Pond near Pattens 
Mills; Vaughns; Shushan; Waterford. 

Cyperus rivularis Kunth. Habitat similar to the preceding 
species;common. Presumably the plant reported as “‘ Cyperus 
Nutiallia Vorr. Luzerne, 1867:/G. W: C(linton)”? m Noes 
State Cab. Rep. 20: 408. 1867 belongs here. 

Cyperus inflecus Muhl. Banks of rivers, vicinity of Cambridge, 
N. Y. (Stevenson). Torrey, Flora of the Northern and Middle 
Sections of the United States, vol. 1: 59. 1824. Furnace 
creek, South Bay, Aug. 20, 1908. 

Cyperus Houghtont Torr. Fort Edward (E. C. Howe); Hague, 
1878 (W. H. Leggett in Columbia Herbarium); sandy fields 
near Bacon Pond; also near the Five Combines, east of Hudson 
Falls. 

Cyperus dentatus Torr. Sandy shores. Trout Pond (C. H. 
Hall); Assembly Point; Bond Pond, Warrensburg; Mud 
Pond; along Hudson River west of Glens Falls. 

Cyperus esculentus L. Cultivated soil. Shushan (F. Dobbin); 
east of Fort Ann; Kingsbury St.; Moss St.; Hudson Falls; 
Coveville; Waterford; Poebles Island, mouth of Mohawk 
River. 

Cyperus strigosus L. Sandy fields and along streams; abundant. 

Cyperus filiculmis Vahl. “Sandy fields, sometimes in rocky 
places; not uncommon. The plants are referable to var. 
macilentus Fernald. 

Eleocharis olivacea Torr. Mud Pond near Pattens Mills, growing 
in miry places. Determined by Dr. C. H. Peck. 

Eleocharis diandra Wright. Hudson River at Bakers Falls, 
Sept. 13, 1899. Determined by Dr. Peck. 

Eleocharis obtusa (Willd.) Schultes. Muddy places, along 
streams and about ponds; common. 


127 


Eleocharis palustris (L.) R. & S. Wet places and shallow water; 
frequent. The var. glaucescens (Willd.) A. Gray is found at- 
Providence (Burt); wet clay bank north of Hudson Falls 
railroad station. Along Hudson River west of Glens Falls; 
and Copeland Pond. Determined by Dr. Peck. The form 
with stout culms, var. vigens Bailey, is found at Bacon and 
Mud Ponds. 

Eleocharis acicularis (L.) R. & S. Stream and pond bottoms, 
where the water has subsided; common. 

Eleocharis tenuis (Willd.) Schultes. Stream banks, bogs and 
about ponds; abundant. 

Eleocharis acuminata (Muhl.) Nees. Shushan (Dobbin). 

Eleocharis intermedia (Muhl.) Schultes. Copeland Pond, de- 
termined by Dr. H. D. House; Shushan, down the Battenkill 
River. 

Stenophyllus capillaris (L.) Britton. Sandy and gravelly soil. 
Day (Peck); slopes of Mt. Defiance (Peck); Fort Edward 
(Howe); Providence (Burt); southwestern W. Fort Ann; 
north of Glens Falls; north of Hudson Falls; Moreau; north- 
west of Waterford; north of Cambridge. 

Fimbristylis autumnalis (L.) R. & S. Mud Pond; moist sandy 
roadside north of Hudson Falls; along Hudson River west of 
Glens Falls. 

Eriophorum alpinum L. Sphagnum marshes. East Lake 
George, at Brayton; marsh near road, north of Glen Lake; 
Rich’s swamp, southwest of Shushan. 

Eriophorum callithric Cham. Sphagnum marshes. North part 
of Salem (Dobbin); E. Lake George; south of Glen Lake; 
Inman Pond. (E. vaginatum of Am. auth.) 

Eriophorum gracile Koch. Lake George (Hall); Shushan, ‘one 
or two mucky situations’? (Dobbin); sphagnum marsh, E. 
Lake George. 

Eriophorum viridicarinatum (Engelm.) Fernald. Sphagnum 
marshes and low swales; frequent. (E. polystachyon of most 
Am. auth.) 

Eriophorum virginicum L. Sphagnum marshes and low swales; 
frequent. The var: album A. Gray often occurs. 


128 


Scirpus subterminalis Torr. Aquatic. Roadside pond, Clemons 
to Black Mt.; Mud Pond; Glen Lake. . 

Scirpus debilis Pursh. ‘‘Luzerne, 1866: G. W. C(linton)” 
in N. Y. State Cab. Rep. 20: 409. 1867. Copeland Pond; 
Hudson River at Bakers Falls; Shushan, down the Battenkill 
River. 

Scirpus Smith A. Gray. Mud Pond near Pattens Mills. 
Determined by Dr. Peck. 

Scirpus americanus Pers. Near the mouth of Pike brook, 
South Bay; Waterford; Poebles Island. 

Scirpus Torreyt Olney. Dresden (Peck). 

Scirpus validus Vahl. Streams and ponds in shallow water; 
common. 

Scirpus occidentalis (S. Wats.) Chase.. Clarks Pond west of 
Shushan. 

Scirpus fluviatilis (Torr.) A. Gray. South Bay, forming swales 
along Dresden trestle north of Whitehall. 

Scirpus sylvaticus L. Low grounds. Fort Ann to Flat Rock; 
northwest Hartford; Moreau, opposite Fort Edward; along 
the trolley, Wilton to Ballston Lake; along the Battenkill 
River south of Shushan. 

Scirpus atrovirens Muhl. Low grounds and moist grassy places; 
abundant. The heads are often proliferous late in the season. 
The form synchocephalus (Cowles) S. F. Blake occurs in Free- 
man’s pasture, Kingsbury St. to Fort Ann. 

Scirpus microcarpus Presl. Low grounds and swamps; frequent. 
‘‘Fine specimens were obtained near Wilton, Saratoga county” 
(Peck).) IN... Y¥. State Mus. Rep: 945: 30.: 1803 ..50nmmeqe 
(S. rubrotinctus Fernald.) 

Scirpus polyphyllus Vahl. Moist woods. Gansevoort (Peck). 
N. Y. State Mus. Rep. 41: 82. 1888. Mt. Hope road north 
of Lake Pond; road to Three Ponds. 

Scirpus Peckit Britton. Shushan (Dobbin). 

Scirpus lineatus Mx. Wet meadows. “Low moist ground 
near Middle Grove’’ (Peck). N. Y. State Mus. Rep. 47: 
30. 1894 Bot. ed. Northwest of Stone schoolhouse, W. Fort 
Ann; Vaughns; near Kingsbury St.; Rosecrans swamp north 


129 


of Glens Falls; along the D. & H. railroad, Ballston to Mechan- 
icsville. : 

Scirpus cyperinus (L.) Kunth. Low grounds, along creeks 
and about ponds; abundant. The var. condensatus Fernald 
is occasionally met with. 

Scirpus pedicellatus Fernald. Lake George (Hall); ‘‘Lake 
Champlain, along railroad between Whitehall and Fort Ann 
and between Schuylerville and Bemus Heights’’ (Peck). 
N. Y. State Mus. Rep. 54: 144. 1901. Fort Ann; W. Fort 
Ann. 

Scirpus atrocinctus Fernald. Whitehall (Peck); W. Fort Ann, 
about ponds; swamp woods, Fort Edward reservoir; An- 
aquassacook meadows, south of Shushan. This species ma- 
tures its fruit earlier than the two preceding species. 

Dulichium arundinaceum (L.) Britton. Borders of sphagnum 
marshes, margins of ponds and wet woods; common. 

Rynchospora alba (L.) Vahl. Sphagnum marshes and borders 
of ponds. Inman Pond; Podunk Pond; Copeland Pond; 
E. Lake George; Glen Lake; Rosecrans swamp; Fort Edward 
reservoir; Rich’s swamp near Shushan. 

Rynchospora capillacea Torr. Along Hudson River west of 
Glens Falls, Sept. 12, 1900. 

Rynchospora glomerata (L.) Vahl. East of South Glens Falls; 
roadside northwest of Hadlock Pond; Copeland Pond. 

Rynchospora fusca (L.) R. & S. Sphagnous border of Dolph 
Pond, west of Comstocks, June 13, 1900 (young). The station 
is probably destroyed. 

Mariscus mariscoides (Muhl.) Kuntze. Borders of ponds. 
Lake George (Hall); Inman Pond; Podunk Pond; Copeland 
Pond; Mud Pond. It has not been seen at the last two stations 
for several years. (Cladiuwm mariscoides (Muhl.) Torr.) 

Carex chordorrhiza Ehrh. Peat bog, Moreau (Howe); E. Lake 
George marsh at Brayton. 

Carex retrofleca Muhl. Peaked Mt.; copse west of Vaughns. 

Carex rosea Schk. Woods and copses; common. The form 
known as var. staminata Pk. occurs at Vaughns and vicinity: 
and the var. radiata Dewey, in northern Washington county. 
Both of these varieties, determined by Dr. Peck. 


130 


Carex convoluta Mackenzie. Silver Bay, Lake George, June 
1901 (J. F. Kemp in Herbarium of N. Y. Botanical Garden). 
Recorded in Bull. Torr. Bot. Club 43: 429. Aug. I9gI5. 
(C. rosea pusilla Pk.) 

Carex cephalophora Muhl. Dry woods; frequent. 

Carex cephaloidea Dewey. Southern base of Woodruff’s hill, 
114 miles west of Fort Ann, June 1892, 1893 (not seen, June, 
1914); woods southwest of Ray Farm, west of Fort Ann, June, 
1904. 

Carex sparganioides Muhl. Copses and rich shaded soil; com- 
mon. The culms are very weak at the time of the falling of 
the perigynia. , : 

Carex vulpinoidea Mx. Low grounds; common. 

Carex xanthocarpa Bicknell. Dry fields and pastures. Gan- 
sevoort and Middle Grove (Peck); southern W. Fort Ann; 
Vaughns. The var. annectens Bicknell is found at Vaughns. 
Determined by Dr. Peck. 

Carex prairea Dewey. East Lake George marsh; Copeland 
Pond; Rich’s swamp near Shushan. Specimens found in 
low grounds, sometimes forming tussocks in shallow water 
at Huletts Landing (Jelliffe); Warrensburg (Peck); Fort 
Edward (Howe); southern W. Fort Ann, formerly known as 
Carex teretiuscula Gooden., have not been verified. Un- 
doubtedly Carex diandra Schrank occurs: but probably the 
majority of our plants are referable to Carex prairea. 

Carex stipita Muhl. Swamps and along streams; common. 
The form known as var. crassicurta Pk. is found in southern 
W. Fort Ann; the var. subsecuta Pk. occurs in Devine’s woods 
at Vaughns and at Tripoli. Both of these varieties were 
determined by Dr. Peck. 

Carex disperma Dewey. Sphagnum bogs and mossy woods; 
frequent. (C. tenella Schk.) 

Carex trisperma Dewey. Sphagnum marshes and cool mossy 
woods; frequent. The var. -Billingsit Knight is found in 
the swamp north of Glen Lake. 

Carex tenuiflora Wahl. Sphagnum marsh, Hartford (Howe); 
E. Lake George marsh at Brayton, June, 1897, and 1900. 
Recorded in N. Y. State Mus. Rep. 54: 161. 1901. 


131 


Carex canescens L. Wet bogs, sphagnum marshes and shaded 
places, rarely in dry woods; frequent. The var. disjuncta 
Fernald is the common form. 

Carex brunnescens (Pers.) Poir. Wet woods, rarely on rocky, 
Southern slopes of Peaked Mt. in loose tufts on rocks; Mott's 
and Dailey’s woods, north of Hudson Falls; Rich’s swamp 
near Shushan. The var. gracilior Britton has been found at 
Inman Pond; bog west of Stone schoolhouse, one mile north 
of Tripoli; Devine’s woods, Vaughns. 

Carex Deweyana Schwein. Copses and rocky woods; common. 

Carex ‘bromoides Schk. Wet woods and along streams, forming 
tussocks; common. 

Carex exilis Dewey. Sphagnum marsh at E. Lake George, 
-Brayton; marsh near the road, north of Glen Lake. 

a ae Willd. Low grounds and sphagnum bogs; abund- 

’The var. . angustata (Carey) was found at Dolph Pond, 

L = 19, 1900; ‘and var. cephalantha (Bailey) in Mott’s woods 

near Hudson Falls, June 28, 1897. Both these varieties were 

determined by Dr. Peck. (Carex sterilis of Am. auth; C. 
stellulata Gooden.) // 

Carex Crawfordit Fernald. Dry and open places. Southern 
W. Fort Ann; rocks at head of Dunham’s Bay, Lake George. 

Carex scoparia Schk. Swales and low meadows; common. 

Carex tribuloides Wahl. Marshy places. Dunham’s Bay; 
Vaughns; Powers Ferry; Fly Kill south of Shushan. The 
forma glomerata Olney from Fort Edward (Howe): and the 
var. turbata Bailey from Middle Grove (Peck), are preserved 
in the N. Y. State Herbarium. 

Carex cristatella Britton. Grassy places near streams and 

ponds; common. 

Carex projecta Mackenzie. Copeland Pond; northeast of 
Tripoli; Devine’s woods; Dailey’s woods. (C. tribuloides 
montliformis Britton.) 

Carex straminea Willd. Dry woods and fields; abundant. 

Carex normalis Mackenzie. Low woods, southern W. Fort 
Ann; Mott’s woods. The var. perlonga (Fernald) is found 
on Haynes hill, Vaughns. (C. mirabilis Dewey.) 


132 


Carex festucacea Schk. Sandy plains northeast of Hudson 
Falls; and gravelly hill north of Copeland Pond. Determined 
by Dr. House. The var. brevior (Dewey) Fernald has been 
found at Warrensburg (Peck); East Galway (Burt); South 
Bay; rocks east of Fort Ann; Peaked Mt.; Peaked Rock, near 
Shushan. 

Carex Bicknellii Britton. Dry sandy soil, East Galway (Burt) 
and Middle Grove (Peck). N. Y. State Mus. Rep. 48: 45. 
1896 Bot. ed. and N. Y. State Mus. Rep. 51: 282. 1898 as 
Carex straminea Crawet Boott. 

Carex foenea Willd. Grassy places, Vaughns, 1893. Deter- 
mined by Dr. Peck. The var. perplexa Bailey has been found 
on ‘‘rocky hills near Whitehall” (Peck). N. Y. State Mus. 
Rep. 46: 52. 1893 Bot. ed. and N. Y. State Mus. Rep. 48: 
44. 1896 Bot. ed. 

Carex leptalea Wahl. Swamps and marshes; frequent. 

Carex pauciflora Lightf. East Lake George marsh at Brayton, 
June 20, 1917. 

Carex communis Bailey. Dry woods and fields; common. The 
var. Wheelert Bailey is found in southern W. Fort Ann and at 
Vaughns. (C. pedicellata (Dewey) Britton.) 

Carex pennsylvanica Lam. Dry woods and fields; abundant. 

Carex varia Muhl. Woods northeast of Tripoli, May 28, 1897. 
Determined by Dr. Peck. 

Carex Novae-Angliae Schwein. Devine’s woods, Vaughns, fer- 
tile spikes 1-4 flowered, May 15, 1897. Determined by Dr. 
neck 

Carex albicans Willd. Warrensburg (Peck). 

Carex umbellata Schk. Dry pastures and sandy fields. East 
of Fort Ann; southern W. Fort Ann; Vaughns; Hudson Falls; 
Crescent. The var. vicina Dewey has been found at Vaughns. 

Carex hirtifolia Mackenzie. Dry woods and thickets. Shushan 
(Dobbin); Vaughns; east of Crescent. (C. pubescens Muhl.) 

Carex pedunculata Muhl. Dry woods and copses; abundant. 

Carex eburnea Boott. Limestone rocks and cliffs. Skene’s 
Mt., Whitehall; northwest Harford; Fort Ann and rocky 
hills 2 miles west; cliffs north of Lake Pond; Long Island, 
Lake George. 


133 


Carex aurea Nutt. Dry hillsides and fields. Southern W. 
Fort Ann; Vaughns; west of Kingsbury St. 2 

Carex plantaginea Lam. Dry hilly and rocky woods, rarely in 
low shaded places; frequent. 

Carex platyphylla Carey. Dry hilly woods; common. 

Carex digitalis Willd. Woods and hillsides. Southern W. 
Fort Ann; Vaughns; Willard Mt. 

Carex laxiculmis Schwein. Grassy woodlands and fields; scarce. 
Vaughns. Determined by Dr. Peck. 

Carex albursina Sheldon. Rich woods and copses. Bacon 
hill, west of Fort Ann; near Tripoli; Vaughns; Anaquassacook 
hills, Shushan. 

Carex blanda Dewey. Lake George (Jelliffe); southern W. Fort 
"Ann; Vaughns. ' The var. varians (Bailey) has been found 
in southern W. Fort Ann; northeast of Glens Falls; Vaughns. 

Carex laxiflora Lam. Grassy places and open places; common. 

Carex anceps Muhl. Shushan (Dobbin); Tripoli; Vaughns. 
(C. laxiflora patulifolia Carey.) 

Carex granularis Muhl. Woods and dry fields; common. 

Carex Hitchcockiana Dewey. Rocky shaded places. Vaughns 
and vicinity. The var. triflora Pk. has been found on Mt. 
Defiance (Peck). N. Y. State Mus. Rep. 46: 51. 1893 Bot. 
ed. and N. Y. State Mus. Rep. 48:66. 1896 Bot. ed. 

Carex conoidea Schk. Grassy places; frequent. 

Carex grisea Wahl. Fields and shaded places; common. 

Carex gracillima Schwein. Woods and fields; abundant. 

Carex prasina Wahl. Grassy and wet places, specially along 
streams. Southern W. Fort Ann; eastern Queensbury; 
Vaughns; east of Crescent. 

Carex formosa Dewey. Grassy banks. Near Vaughns school- 
house; 14 mile east of Tripoli. Determined by Dr. Peck. 

Carex flexuosa Muhl. Woods; frequent. (C. tenuis Rudge.) 

Carex arctata Boott. Moist woods.. Mt. Defiance (Peck); 
Silver Bay (Kemp, in Herbarium of N. Y. Botanical Garden) ; 
Providence, also path to Lake Desolation (Burt); Fort Ed- 
ward (Howe); near the falls, West brook, W. Fort Ann. 

Carex castanea Wahl. Grassy places; rare. Fencerow 14% 


134 


miles east of Vaughns, June 1892, 1893; woods west of Smiths 
Basin. 

Carex Sprengelut Dewey. Shaded places, usually calcareous 
rocks; rare. Mechanicsville (Peck); Shushan (Dobbin); 
Haynes hill and in woods west of Vaughns. (C. longirostris 
Morr) 

Carex Swanu (Fernald) Mackenzie. Dry pastures and woods. 
Vaughns; Shushan; north of Cambridge. 

Carex virescens Muhl. Dry hilly woods. Warrensburg (Peck); 
Crosset Pond; southern W. Fort Ann. 

Carex complanata Torr. Old pastures and dry open woods; 
abundant. (C. triceps Mx.) 

Carex complanta Torr., var. robusta var. nov. 

Culms rather stout, erect, 15’—3° tall; leaves 114-3” wide; 
spikes 2 (rarely 3), oblong, very dense, 3’’-12”’ long, 3/’-5”” in 
diameter, the terminal one conspicuously staminate at the 
base; scales brownish, scarious-margined, as long as or ex- 
ceeding the few but distinctly nerved perigynia. 

This distinct variety grows with the species, in the north- 
west corner of Alaric Freeman’s meadow, next to Charles 
Bentley’s pasture, about 1 mile north of Kingsbury Street. 
It was first found June 18, 1892 and several tufts of plants 
were seen in 1918. It matures a week or twoearlier than the 
species. 

“A form with oblong spikes. Mt. Defiance” (Peck) is 
probably referable to this variety. N.Y. State Mus. Rep. 34: 

S564) aS Siel: 

Carex pallescens L. Clayey meadows and open woods; fre- 
quent. 

Carex scabrata Schwein. Cold swamps and along mountain 
streams; frequent. 

Carex limosa L. Southern part of E. Lake George marsh, June 
20, 10X75 

Carex paupercula Mx. Sphagnum marshes. The plants are 
referable to the var. irrigua (Wahl.) Fernald. Hartford 
(Howe); E. Lake George; marsh north of Glen Lake; Inman 
Pond. (C. magellanica of Am. auth.) 


135 


Carex stricta Lam. Wet places, forming tussocks in shallow 
water; common. The var. angustata (Boott) Bailey some- 
times occurs with the species. 

Carex torta Boott. Shushan (Dobbin). Determined by Dr. 
Peck. Rocky bank of Battenkill River at East Salem, June 
15, 1907. 

Carex gynandra Schwein. Middle Grove (Peck); eastern 
Queensbury. 

Carex crinita Lam. Along streams, marshes and borders of 
ponds; common. 

e Carex lacustris Willd. Low grounds and about ponds forming 
swales; common. The plants are usually sterile. (C. riparia 
of Am. auth.) 

Carex vestita Willd. Sandy clearing in Five Combine woods, 
east of Hudson Falls, June 2, 1892. 

Carex lanuginosa Mx. Wet field, north of Hudson Falls, near 
Tefft’s corner, May 23, 1896. 

Carex lasiocarpa Ehrh. About ponds and mossy bogs; frequent. 
(C. filiformis of Am. auth.) 

Carex Houghtonit Torr. Sandy field near Shield’s estate, East 
Galway, July 11, 1880 (Burt). This is also recorded in N. Y. 
State Mus. Rep. 47: 41. 1894 Bot. ed.; N: Y. State Mus. 
Rep. 48: 87-88. 1896 Bot. ed.; and N. Y. State Mus. Bull. 
176: 23. I9QI5.:- 

Carex trichocarpa Muhl. Shushan (Dobbin). 

Carex cryptolepis Mackenzie. Marsh north of Podunk Pond; 
Dolph Pond. Carex flava, var. graminis Bailey, with erect 
bracts has been found at Warrensburg (Peck). (C. lepidocarpa 
Tausch.) 

Carex flava L. Wet places and low meadows; common. 

Carex folliculata L. Wet woods. Moreau (Howe); Galway 
(Burt) ; near Fort Edward reservoir, probably Howe’s station; 
Five Combine woods and Dailey’s woods, near Hudson Falls. 

Carex monile Tuck. Wet places, often in water. Lake Desola- 
tion (Burt); Mud Pond near Pattens Mills; Flat Rock near 
Fort Ann; Dailey’s woods; Anaquassacook meadows, south 
of Shushan. 


136 


Carex rostrata Stokes. Wet bogs. Shushan (Dobbin); Dolph 
Pond; New Michigan Pond ‘‘Talman marsh.’’ Not rare at 
Copeland Pond; determined by Dr. House. (C. utriculata 
Boott.) 

Carex Tuckermanit Dewey. Wet shaded places; uncommon. 
Assembly Point (Dr. Geo. D. Hulst, in Herbarium of Brooklyn 
Botanic Garden); Huletts Landing (Jelliffe); Mechanicsville 
(Peck); between Copeland and Hadlock Ponds; northwest 
Hartford; Dailey’s woods; copse north of Devine’s woods, 
Vaughns; along Battenkill River south of Shushan. 

Carex retrorsa Schwein. Wet places; frequent. The var. Harti 
(Dewey) Gray was found north of Vaughns, Sept. 4, 1891. 

Carex lurida Wahl. Wet places; abundant. 

Carex Baileyi Britton. Shaded swamps. Lake George (Hall); 
along road between Chestertown and Warrensburg (Peck); 
Lake George to Warrensburg; lower Black Mt. trail from 
Clemens; Dailey’s woods. 

Carex hystricina Muhl. Wet places; common. The var. 
Dudleyi Bailey has been found at Galway (Burt). 

Carex Pseudo-Cyperus L. Lake Lauderdale, July 3, 1904. 

Carex comosa Boott. Borders of ponds and marshes; frequent. 

Carex intumescens Rudge. Wet woods, moist fields and swamps; 
common. The var. Fernaldi Bailey has been found in the 
copse north of Devine’s woods; woods north of Cambridge. 

Carex Asa-Grayi Bailey. Wet places in Devine’s woods, Vaughns. 

Carex lupulina Muhl. Wet places; common. The var. Bella- 
villa (Dewey) Bailey has been found at South Ballston (Peck). 
The var. pedunculata Dewey is occasionally found with the 
species. 

Carex lupulina X retrorsa Dudley. South Ballston (Peck). 
Specimen in N. Y. State Herbarium. 

Carex lurida X lupulina Bailey. Charlton. N.Y. State Mus. 
Rep. 33: 35. 1880 as Carex tentaculata, var. altior Boott. 


Specimen in N. Y. State Herbarium. 
Hupson FA ts, N. Y. 


137 


SOME WESTERN COLUMBINES 
By T. D. A. COCKERELL 


Last year (Contrib. U. S. Nat. Herbarium, 20: Part 4) Mr. E. 
B. Payson published a most interesting revision of the genus 
Aquilegia as found in North America, and this will naturally 
serve as a point of departure for new investigations. The sub- 
ject is a difficult one, owing to the fact (as it seems to be) that 
any species in the genus will freely cross with any other; and, at 
least in our experience, the hybrids themselves are perfectly 
fertile. Thus, on grounds similar to those which convince us 
that there is only one living species of Homo, it may be main- 
tained that there is possibly only one genuine species of A quilegia. 
Nor is this all; just as Bursa bursa-pastoris var. heegeri (commonly 
called Bursa heegert) is a form lacking the most prominent 
character of the genus to which it belongs,* so Aquilegia vulgaris 
var. stellata and A. caerulea var. datleyae lack the generic character 
of spurred petals, so that but for their obvious general affinities 
we might not regard them as columbines at all. This plasticity 
is remarkable in a genus which in many respects seems highly 
modified. The long spurs are adapted to the visits of butter- 
flies, but I have seen a bumble-bee (Bombus) slit up a spur from 
the side, and thus get at the nectar illegitimately. The colum- 
bine in which this occurred was A. caerulea. Mr. Payson sug- 
gests that ‘‘the modern species of Aquilegia seem to have been 
developed from species having blue flowers. These seem first 
to have given rise to white-flowered, these to yellow-flowered, 
and these finally to red-flowered species.’’ There is apparently 
no basis for such an evolutionary sequence, for the yellow in 
the flowers is due to plastids, readily visible under the microscope; 
while the blue and red are equally due to anthocyanins, held in 
solution in the sap. Gaston Bonnier, in his scheme of relation- 
ships of Ranunculaceous genera, indicates an affinity between 
Aquilegia and Helleborus, while the latter leads back to Caltha, 
etc. The suggestion might be, that the original columbines were 


* For a good figure, see Shull, Zeits. f. indukt. Abstamm. u. Vererbungslehre. 
12:98. I914. 


138 


yellow or white, if there was any well marked sequence in the 
evolution of color. Purple, however, is already a prominent 
color in species of Helleborus, and it is evident that anthocyanins 
and yellow plastids both antedate the evolution of Aquilegia. 

A few years ago* I described a hybrid between A.desertorum and 
A. chrysantha. Our plant of A. desertorum, obtained in Santa 
Fé Cafion in 1912, and then evidently of considerable age, is as 
vigorous as ever in 1919. It proves fertile with its own pollen, 
and we have seedlings from it already in flower, perfectly true 
to type. It has been and still is a question whether the differ- 
ences between A. desertorum and A. elegantula may be due to 
environment and hence not truly specific. Mr. Payson treats 
them as distinct species, but declares that desertorum is known 
only from Arizona, though he quotes my remarks on the New 
Mexico plant. A specimen obtained by Heller nine miles east 
of Santa Fé, and therefore very near the locality of my desertorum 
plant, is referred by Payson to elegantula. An analysis of the 
characters of my plant, with Payson’s descriptions before me, 
appears to indicate desertorum rather than elegantula, but it 
agrees perfectly with neither. The leaves are early glaucous, 
but at maturity clear green above. Only the leaflets of the 
flowering stems are small; the basal leaves have them very large, 
the apical leaflet 40 mm. long and 38 wide. The better developed 
flowering stems bear well-developed leaves, but this can hardly 
be a specific character. The leaflets have a quite dense erect 
pubescence on the under side, which is a desertorum character. 
(A. chrysantha has this pubescence less dense, but still very evi- 
dent; but singularly enough the chrysantha X desertorum hybrid 
has only a very few widely scattered hairs.) The spurs are 
about 22 mm. long, thus agreeing better with desertorum, and 
the sepals are red, pallid at tip. The original elegantula, as 
described by Greene, had light green sepals. The sepals how- 
ever are erect, not spreading as they should be in desertorum. 
The follicles have the tips widely spreading. 

On the basis of the above characters, it might appear that the 
Santa Fé Cafion desertorum should be separated both from the 


’ * Botanical Gazette 62: 413. 1916. 


139 


true desertorum of Arizona and the typical elegantula from near 
Mancos, Colorado. It seems more probable, however, that 
all three represent phases of a single species. Mr. D. M. Andrews 
has recently collected elegantula in Colorado, and thinks that it 
is separable from my plant on account of the habit of growth. 
We do not yet know how far this may be due to differences in 
environment. 

The F, plants from desertorum X chrysantha, raised by my wife, 
flowered this year. The most curious form shows doubling, 
with twisting of the spurs. The spurs vary from 6 to 9, but the 
laminae of the petals are supplemented internally by a variable 
number of emarginate laminiform appendages. 

This year we have an authentic A. caerulea X desertorum in 
flower. The flowers are formed as in caerulea, with pure white 
laminae; but are smaller, the sepals pale lilac tipped with white, 
the spurs rosy-lilac. In bud the spurs are suffused with red. 
The leaflets are pubescent beneath, the hair short but abundant. 
Spurs 28 mm. long, laminae 11 mm; sepals about 20 mm. long 
and a little over 8 mm. wide. In full flower the spurs are moder- 
ately divergent. The leaflets are large, even on the flowering 
stems. 

We also have this year a varied series of F2 plants from A. 
caerulea X chrysantha. A. chrysantha has yellow flowers, often 
with some anthocyan tints, which then are red, but never sufh- 
ciently to affect the general yellow effect. The sepals are pre- 
vailingly narrower than in caerulea, but variable. The F; from 
caerulea X chrysantha is pale blue with the laminae yellow, fading 
to nearly white. The F, plants include such as the following: 

(a) Form of caerulea, with broad sepals, but laminae entirely 
bright lemon yellow; sepals dilute rosy purplish, more or less 
suffused with yellow, especially at tips; spurs pale yellow, apically 
suffused with dilute purplish; buds strongly pinkish, including 
spurs. Thus the buds show the acid state of the anthocyanin, 
which is retained to maturity in chrysantha, but the hybrid is 
affected by the caerulea ancestry. This type of F: hybrid occurs 
only in a small percentage of the plants. 

(b) Sepals broad as in caerulea; flowers white, very delicately 
tinted with purple on sepals and often on spurs. 


140 


(c) Similar to the above, but with less of the purplish tint 
(more on spurs), and the whole flower (especially laminae) is 
very pale yellow. Others show more of the purplish and brighter 
yellow, intermediate between a and c. 

The factorial analysis of these forms cannot yet be clearly 
made. A. caerulea in the western part of its range is not blue but 
white, but there is no evidence that the plants we used carried a 
recessive white. Wecan however postulate that yellow plastids 
(chrysantha) are allelomorphic to their absence (caerulea), and 
abundant anthocyanin (caerulea) to little or none (chrysantha). 
It we call the factors respectively P, p, A, a, the F; hybrid will 
have the formula PpAa, and will combine blue with yellow, as 
it actually does, with non-acidity also dominant over the acid 
condition of chrysantha. In the F2 9 out of 16 should look like 
the F,; three should resemble caerulea, three chrysantha, and one 
might be expected to be white, feebly or not tinted with antho- 
cyanin. Evidently other factors are involved, for as a matter 
of fact the pallid (supposedly double recessive) flowers are 
numerous. 

Genuine A. caerulea produces some hitherto unrecorded 
variations. Mr. D. M. Andrews has at Boulder, Colorado, a 
large stand of very fine and typical caerulea, the seed having 
been obtained from the Blanchard ranch in Boulder Cafion. 
The strain originated in the nearby mountains, and is in general 
extremely uniform. But as Mr. Andrews pointed out to me, 
there are a few plants abruptly and conspicuously varying from 
the type: 

1. Laminae of petals blue like the sepals, elongate, narrow 
(e.g., 40 mm. long and 8 wide); spurs normal, varymg to small 
and more or less aborted. A few plants. This is more or less 
intermediate between the typical form and variety dazleyae, 
but distinct from both. 

2. Flowers very pale, light yellowish or greenish in bud, 
eventually delicately tinted with. purplish. Sepals and petals 
9 to 10, the sepals reflected at maturity, placed just below the 
outwardly-turned spurs; laminae remaining erect, lanceolate, 
about as long (20 mm.) as the spurs. The sepals are mainly 


141 


pale green, the laminae delicate purplish one plant only. This 
has an atavistic appearance, and is quite without the beauty of 
normal caerulea. , 

These observations indicate that Aquilegia is an unusually 
favorable genus for the investigation of genetic problems. Some 
of its advantages are the following: (1) The ready hybridization 
and fertility of the F,; (2) the tendency to mutate, apart from 
crossing; (3) the existence of spurred and spurless forms, and of 
forms with and without colored plastids and anthocyanin colors; 
(4) the heterozygotes can be easily preserved and propagated by 
dividing the crowns; (5) incidentally, beautiful and interesting 
garden plants are produced. 


SHORTER NOTES 


Rhamnus dahurica 1x MicuicAN.—South of Ann Arbor, 
Michigan, is an extensive area of level ground formerly occupied 
chiefly by tamarack, black ash, and other hydrophytic trees. 
The ground water lies always near the surface and parts of the 
area were originally very swampy. Recent construction of 
drainage systems has destroyed much of the swamp, which has 
been put under cultivation, but the rest of the tract is still in 
forest. 

Five years ago a forestry class of the University of Michigan 
discovered in the heart of the swamp a tree unknown to them. 
It was submitted to the writer for identification and proved to 
be Rhamnus dahurica. It was then supposed that the tree had 
been planted by Mr. J. B. Steere, who owns part of the land and 
had travelled extensively in the Orient. In 1916 Mr. Steere 
pointed out a second tree to the writer, some two miles from the 
first one, with a request for its identification. He was surprised 
to learn its name and disclaimed any knowledge of its origin. 
Only one tree of the species is known in cultivation in the vicinity, 

which, since it is a smaller tree, can scarcely be considered as the 
_ parent of these two individuals. 

The two apparently wild trees are 500 yards or more from any 

residence, either past or present. One is in the middle of a forest 


142 


tract; the other along a small ditch separating two cultivated 
fields, but it obviously antedates the construction of the ditch. 
Each is about thirty feet high, with widely spreading branches 
in healthy condition, and bears a good crop of fruit. Seedlings 
have not been seen.—H. A. GLEASON. 


NEWS ITEMS 


According to The Cambridge Tribune of June 28, Harvard 
University benefits from the will of the late Dr. W. G. Farlow, 
professor emeritus of cryptogamic botany. All of his books, 
papers, manuscripts, etc., are left to the University, to constitute 
the Farlow Reference Library. The sum of $25,000 is left in 
trust to his assistant, A. B. Seymour, who will enjoy its income 
during his life. On his death this fund will be added to a gift 
of $100,000 previously made to Harvard and known as the John 
S. Farlow Memorial Fund. On the death of Professor Farlow’s 
widow, $100,000 will be given to the University and added to 
the John S. Farlow Memorial Fund. 


In connection with the commencement exercises of the Uni- 
versity of Vermont, held in Burlington on June 25, the degree 
of doctor of letters was conferred upon Dr. Liberty Hyde Bailey, 
formerly director of the College of Agriculture of Cornell Uni- 
versity, and the honorary degree of doctor of science was con- 
ferred upon Dr. Marshall Avery Howe, curator of the museums 
of the New York Botanical Garden. 


Dr. H. N. Whitford, of the School of Forestry of Yale Uni- 
versity, has recently returned from Central America, where he 
was one of a commission detailed by the State Department to 
investigate the economic resources of the boundary region in 
dispute between Guatemala and Honduras. 


_ The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of TorREYA in which their papers appear, will kindly notify the 
editor when returning proof. 7 

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Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs. E. G. BRITTON, Chairman. 
J. H. BARNHART, Pror. JEAN BROADHURST 
Miss C. C. HAYNES B. O. DoDGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F. J. SEAVER 


Membership Committee 


J. H. BARNHART, Chairman. 
J. K. SMALL, Chairman. 


R. A. HARPER 

N. L. BRITTON T. E, HAZEN 

A. W. Evans E. W. OLIVE 

M. A. Howe Local Flora Committee 

H. H. Russy N. L. Britton, Chairman. 

Field Committee Phanerogams: Cryptogams: 

F. W. PENNELL, Chairman. E. P. BICKNELL Mrs. E.G. BRITTON 
Mrs. L. M. KEELER N. L. BRITTON T. E. HAZEN 
MICHAEL LEVINE C. C. CurTIS M. A. Howe 
GEORGE T. HASTINGS K, K. MACKENZIE MICHAEL LEVINE 
PERCY WILSON NORMAN TAYLOR W. A. MuRRILL 


F. J. SEAVER 
Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill ' Imperfecti: H. M. Richards, F. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurs 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


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Vol. 19 August, 1919 No. 8 


TORREYA > 


A Monruty Journat or BoranicaLt Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873. 


CONTENTS 
Scrophulariaceae of the Local Flora II: F. W. PENNELL.. ccecscspecsceteeneeeetecereueeee 143 
Reminiscences of Orchid-Hunting: HERBERT M. DBNSLOW.....esee-seeseeee snes ee eceere 152 
Prncroa ino Of tite Club. .:; 2d... cbecavudewacasigeboty caveretset tren oop da caduaeh smc ah -antisace 157 
ONE ELON os Sen cas cade) brah Se thawa Sitaesaithe undslp rahe AN cd tae Spee evasion dfocgeakdenvon anv en’ 156 


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THE TORREY BOTANICAL CLUB 


OFFICERS FOR 1919 


President 
H. M. RICHARDS, Sc.D. 


¥ Vice- Presidents. 
JOHN. HENDLEY BARNHART, A.M., M.D | 
C. STUART GAGER, PH.D. 


Secretary and Treasurer 
BERNARD O. DODGE, Pu.D. 
CoLtumMBIA UNIversITy, N. Y. City. 
Editor ; 
ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


JEAN BROADHURST, Pu.D. M. LEVINE, Pu.D. 
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MARSHALL AVERY HOWE, Pu.D. ARLOW B. STOUT, PH.D. 


NORMAN TAYLOR. 


Delegate to the Council of the New York Academy of Sciences 
M.A. HOWE, PH.D. 


OFFICIAL ORGAN OF THE WILD FLOWER PRESERVATION 


SocieTY OF AMERICA 


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TORREYA 


Vol. Ig No. 8 
August, IgIg 


SCROPHULARIACEAE OF THE LOCAL FLORA. II 
By Francis W. PENNELL 
Continued from June TORREYA 


5. LIMOSEEEA, L, Sp. Pl. 620.. 41753- 
Type species, L. aquatica L., of Europe. 


1. LIMOSELLA SUBULATA Ives in Trans. Phys. Med. Soc. N. Y. 


1:440. 1817. ‘‘Firstobservedin 1816. . . It flourishes 
in great abundance in the Housatonic, and in most of 
the rivers which empty into Long Island Sound, within 
the range of the tide.”’ 

Ygramela (or Limosella) maritima Raf. Atl. Journ. 199. 
1833. ‘‘ Discovered this year in the wet sand of the sea 
islands of New Jersey.’”’ As a new genus, this was based 
upon specimens the flowers of which bore but two stamens. 
Certainly an abnormal form, as the plant of such situa- 
tions has normally four stamens. 

Flowering from late August to November, and soon ripening 
fruit. 

Tide-water river-beaches, saline, brackish or fresh, and about 
borders of ponds, brackish or fresh, along the coast. Margins 
of ponds back of sand-dunes, growing inundated or somewhat 


- emersed on the sandy coastward margin of these, Long Island 


and southward to Ocean County, New Jersey; on the sandy or 
gravelly flats between high and low tide, along the Housatonic, 
Hudson, Passaic, Delaware, and doubtless other rivers. The 
plants of the two environments differ slightly, as has been indi- 
cated in Torreya 19: 51. 1919. This species ranges from 
Labrador to Maryland. 


[No. 7, Vol. 19 of TorrEnYA, comprising pp. 125-142, was issued Sept. 10, 1919] 


145 


144 


6. GRATIOLACIS Spe Plt 7s i 753. 
Type species, G. officinalis L., of Europe. 


Corolla slightly exceeding calyx, externally glabrous. 
Capsule nearly pyramidal, acuminate. Pedicels very 
short. Stem pubescent with several-celled hairs. (Pilosae.) 1. G. pilosa 
Corolla more than twice as long as the calyx, externally more 
or less puberulent. Capsule broader, acute to rounded. 
Pedicels longer. Stem glabrous or puberulent with one- 
celled hairs, these frequently gland-bearing. 
Pedicels exceeding 10 mm. in length. Corolla within 
throat on posterior side densely pubescent with 
knobbed hairs. Capsule ovate, equaled or ex- 
ceeded by the sepals. Seeds 3-5 mm. long, semi- 
globose to oblong. 
Capsule 1-3 mm. long, exceeded by the sepals. 
Stem-leaves clasping by a broad base, usually at 
least the upper with resinous dots. Roots 
perennial, slender. Stoloniferous. (Ramosae.) 
Corolla golden-yellow throughout. Capsule 
3 mm. long, little exceeded by the sepals. 
Leaves lanceolate to nearly ovate, entire or 
distally obscurely denticulate, with blackish 
glandular dots. 
Leaves linear to lanceolate, frequently denti- 
culate distally, usually strongly puncticulate. 
Sepals obtusish to acute. 2. G. aurea. 
Leaves lanceolate to nearly ovate, entire, ob- 
scurely puncticulate distally. Sepals very 
obtuse. 2a. G. aurea obtusa, 
Corolla with throat dull-yellow, the lobes white. 
Capsule 2 mm. long, much exceeded by the 
sepals. Leaves ovate, serrate, the upper some- 
times with sparse glandular dots. 3. G. viscidula. 
Capsule 4-5 mm. long, about equaled by the sepals. 
Stem-leaves narrowed to a sessile or slightly clasping 
base, not resinous-dotted. Roots annual, the 
main root thick and giving off numerous fibers. 
Not stoloniferous. (Neglectae.) 4. G. neglecta. 
Pedicels less than 5 mm. in length. Corolla within 
throat on posterior side pubescent with knobless 
hairs. Capsule globose, 5-6 mm. long, slightly ex- 
ceeding the sepals. Seeds 7 mm. long, linear. Leaves 
and root as in Neglectae. (Virginianae.) 5. G. virginiana. 


I. GRATIOLA PILOSA Michx. Fl. Bor. Am. 1: 7. 1803. ‘Hab. 
in Carolinae inferioris uliginosis.’’ Description suffici- 
ently distinctive. 


145 


Sophronanthe pilosa (Michx.) Small, Fl. S.E. Un. St. 1067, - 
1338. 1903. 

Flowering mid-July to late September, and soon ripening 
fruit. 

Moist sandy pineland, in potassic soil, Cape May District 
and locally in Camden County in the Middle District, of the 
Coastal Plain of southern New Jersey. Ranges from New Jersey 
to Florida and eastern Texas, in the Coastal Plain. < 
SeSRATIOLA AUREA Pursh,; Fl. ‘Am. Sept: 1i‘12. "1814. “In 

sandy wet places, in the pine-barrens of New England, 
New Jersey and Carolina ... v. v.; v. s. in Herbario 
Banksiano.’’ Description distinctive, here restricted to 
the northern first-mentioned plant. 

Flowering from early June to late September, and soon ripen- 
ing fruit. Apparently fruit is sparingly matured, the plant 
increasing mainly by stolons. 

Wet sandy potassic soil, margins of ponds; frequent in the 
Coastal Plain of Long Island and New Jersey, especially in the 
Pine Barrens; occasional about lakes in the glaciated region 
above the Fall-line, at least at Lake Hopatcong, Morris Co., New 
Jersey. Ranges from Maine and eastern Ontario to Virginia. 
2a. Gratiola aurea obtusa Pennell, var. nov. 


Plant erect, 1.5 dm. tall. Leaves lanceolate to ovate, 1.5 cm. 
long, entire, obscurely puncticulate distally. Sepals 3 mm. 
long, very obtuse. Corolla 10-12 mm. long. 


Type, gravelly shores of Delaware River, between high and 
low tide, Fish House, Camden Co., New Jersey, collected in 
flower by Stewardson Brown; in herb. Academy of Natural 
Sciences of Philadelphia. 

Gravelly or sandy shores of Delaware River, between tides, 
Mercer and Camden counties, New Jersey, and Philadelphia 
Co., Pennsylvania. 

3. Gratiola viscidula Pennell, nom. nov. 

Gratiola viscosa Schwein.; Le Conte in Ann. Lyc. N. Y. 1: 
106. 1824. ‘“‘Inhabits Virginia, and the upper parts of 
North Carolina.”” Apparently the plant now considered, 
although the description appears inaccurate in stating 


146 


that the capsule is as long as the sepals. Not G. viscosa 
Hornem. Enum. Pl. Hort. Hafn. 19. 1807. 

Flowering from mid-July to September, and soon ripening 
fruit. 

Swales and swamps, along streams, in potassic soil, at a few 
stations in the Piedmont of northern Delaware. Ranges from 
Delaware to upland Georgia and eastern Tennessee. 

4. GRATIOLA NEGLECTA Torr. Cat. Pl. N. Y.89. 1819. “With- 
in thirty miles of the City of New York.” In the her- 
barium of Columbia University are two sheets, probably 
representing but one collection, both labeled “Gratiola 
virginica Linn., Torr. Fl. N. Y., 2, p. 37.”’ It is possible 
that one or both of these are Torrey’s plants of G. neglecta. 
The latter was described as distinct from G. virginiana 
because of the lack of the rudimentary antero-lateral 
filaments. Five years later, in his Flora of the Northern 
States, Torrey was persuaded that this lack was true of 
G. virginiana, and on that account reduced his earlier 
species. Still later, in 1843, in his Flora of New York, 
he described such rudiments as present, and held as 
erroneous his previous observations. The truth, as 
confirmed by an extensive examination of fresh flowers, 
is that these rudiments may be small, or reduced to one, 
or altogether absent; all stages are to be found in the 
same colony. The name is here used for the species 
which has long been known as G. virginiana. 

Conobea borealis Spreng. in Neue Entdeck. 3: 26. 1822. “Hab. 
in locis humidis. prope Noveboracum. ...’’ This is 
virtually a. re-description of Gratiola neglecta Torr., 
although sufficient new matter is added to indicate that 
Sprengel must have seen a specimen of this. The change 
of generic classification is doubtless due to the discovery 
of sterile rudiments of the antero-lateral filaments. 

Flowering from late May to late September, and soon ripen- 
ing fruit. ! 

Wet loam, woodland or open, in potassic soil, common above 
the Fall-line; and through the Middle District of the Coastal 


147 


Plain. Ranges from Maine and Quebec to British Columbia, 

southward to Georgia, Texas and California. 

5. GRATIOLA VIRGINIANA L. Sp. Pl. 17. 1753. ‘Habitat in 
Virginia.”” Although Linné had specimens of the plants 
here called G. neglecta in his herbarium in 1753, his de- 
scription is taken solely from Gron. Fl. Virg. 6, 1743, and 
so is based upon Clayton 379. ‘This, as shown by Dr. S. 
F. Blake in Rhodora 20:65, 1918, is the plant which has 
been known as G. sphaerocarpa Ell. 

Flowering from mid-May to September, and soon ripening 
fruit. . 
Wet loam, in shade, occasional in the Middle and Cape May 
Districts of the Coastal Plain of New Jersey, and below the Fall- 
ine in Delaware. From Burlington, N.J. southward to Florida 

and Texas, extending inland to the southern Appalachians. 


72 MuMuULUS: IL Sp, Pl 6345 1753 
Type species, M. ringens L. 


Corolla yellow. Capsule dehiscent laterally, apex persistent and 
valves permanently attached to axial cell-wall. Seeds ellip- 
soid-orbicular. Stems pubescent. Species introduced. 

(Simiolus Greene.) 
Corolla 12-20 mm. long. Leaves 3-4 cm. long. Stems 


loosely lanose, slender, lax. 1. M. moschatus 
Corolla 30-35 mm. long. Leaves 4-5 cm. long. Stems 
glabrous to finely glandular-pubescent, stout, erect. 2. M. guttatus. 


Corolla lavender-violet. Capsule dehiscent laterally from very 
apex, and its valves splitting from the persistent axial cell- 
wall. Seeds oblong. Stems glabrous. Species native. 
(Eumimulus.) 
Leaves ovate, petioled. Angles of stem slightly winged. 
Pedicels stout, in fruit 5-10 mm. long. Calyx-lobes seta- 
ceous-tipped, 1-2 mm. long. Corolla 35 mm. long. 
Seeds pale-yellow. 3. M. alatus. 
Leaves lanceolate, clasping. Angles of stem not winged. 
Pedicels slender, in fruit 30-60 mm. long. Calyx-lobes lan- 
ceolate, 3-5 mm. long. Corolla 30 mm. long. Seeds 
brownish. 4. M. ringens. 


1. MIMULUS MOSCHATUS Dougl. 


Aquatic in running streamlets or in bogs; rare; seen only from 
Queens and Sullivan counties, New York and Lehigh County, 


148 


Pennsylvania. Certainly an escape from cultivation on Long 

Island, but in the mountain habitats it appearsas if native. A 

native of the Rocky Mountains, occurring eastward in northern 

Michigan, Newfoundland and northern New England. 

2. MIMULUs GuTTATUS DC. 

Meadows and along streams, rarely escaped from cultivation; 
seen from Litchfield County, Connecticut, and Delaware County, 
New York. Native of western North America. 

3. MIMuULUS aLatus Ait. Hort. Kew. 2: 361. 1789. “Nat. 
of North America. Introd. 1783, by Mr. William Mal- 
colm.”’ 

Flowering from late July to early September, and soon ripen- 
ing fruit. 

Shaded swamps and along streams, in potassic soil, frequent, 
becoming rare northward, through the area above the Fall-line; 
occasional in the Middle District of the Coastal Plain of New 
Jersey. Ranges from Connecticut to Ontario and Kansas, 
southward to Florida and Louisiana. 


4. MIMULUS RINGENS L. Sp. Pl. 634. 1753. ‘“‘Habitat in Vir- 


ginia, Canada .. . Hort. ups.176:t.2.’ Inthe Hortus 
Upsalensis 176, pl. 1, 1748, Linné described and figured 
our plant. ; 


Flowering from early July to mid-September, and soon ripen- 
ing fruit. 

Open swales and along streams, more rarely in shaded swamps, 
in potassic and calcareous soils, common throughout the area 
above the Fall-line, of more rare occurrence through the Middle 
District and Coast Strip of the Coastal Plain. Ranges from 
Nova Scotia to Alabama, Minnesota and Kansas. 


8. ILYSANTHES Raf. Ann. Nat. 13. 1820 
Type species, I. riparia Raf., of the Ohio valley. 


Leaves 1-3 cm. long, obviously attenuate at base. Pedi- 
cels relatively stout, at least in fruit, shorter than the 
bracts. Sepals usually finely pubescent, usually about 
equaling the capsule. 
Leaves lanceolate to ovate-lanceolate, usually only the 
lowermost obtuse. Fruiting pedicels 5-10 mm. 
long. Plant diffuse. 1. I. dubia. 


149 


Leaves elliptic-oval, all obtuse. Fruiting pedicels 

3-5 mm. long. Plant erect. ta. I. dubia inundata- 
Leaves .5—1.5 cm. long, rounded at base, or at least broadest 

much below the middle. Pedicels filiform, longer than 

the bracts. Sepals glabrous or nearly so, shorter than 

the capsule. 2. I. inaequalis. 

I. ILYSANTHES DUBIA (L.) Barnhart. 

Gratiola dubia L. Sp. Pl. 17. 1753. ‘‘Habitat in Virginiae 
aquosis.” Type, Clayton 164, identified by Dr. B. L. 
Robinson in Rhodora 10: 67. 1908, as the species here 
considered. 

Capraria gratioloides L. Syst. ed. X. 1117. 1759. Based 
upon Gratiola dubia L. 

Ilysanthes gratioloides (L.) Benth. in DC. Prod. 10: 419. 
1846. 

Lindernia gratioloides (L.) Lloyd & Fouc. Fl. Ouest Fr. ed. 
IV. 246. 1886. 

Ilysanthes dubia (L.) Barnhart in Bull. Torr. Club 26: 376. 
1899. 

Flowering from early July to October, and soon ripening 
fruit. 

Swamps, in potassic soil, frequent above the Fall-line and in 
Middle and Cape May Districts of the Coastal Plain. Ranges 
from New Brunswick and Ontario to Florida and Texas. 
1a. Ilysanthes dubia inundata Pennell, var. nov. 

Plant erect, 1.5-2 dm. tall. Leaves elliptic-ova!, obtuse, 1.5- 
2cm.long  Pedicels in fruit but 3-5 mm. long. 

Type, sandy tidal flats of Delaware River above Delair, Cam- 
den Co., New Jersey, collected in fruit September 3, 1915, 
Pennell 6496; in herbarium New York Botanical Garden. 

Tidal flats of Passaic River, New Jersey, of the Delaware 
River in New Jersey, Pennsylvania and Delaware. Also seen 
from along the Potomac River near Alexandria, Virginia. 

2. Ilysanthes inaequalis (Walt.) Pennell, comb. nov. 

Gratiola inaequalis Walt. Fl. Carol. 61. 1788. Probably 
from lower South Carolina, a district where the plant 
here considered is frequent. Identified by Michaux, 
Fl. Bor. Am. 1:7. 1803 as questionably his own Gratiola 


150 


anagallidea, and by Elliott, Sketch Bot. S. C. & Ga. 1: 
16. 1816, identified and carefully described under the 
name Lindernia dilatata Muhl. Both the latter specific 
names are synonyms of this. 

Flowering from late June to late September, and soon ripening 
fruit. 

Swamps, in potassic soil, frequent throughout the Coastal 
Plain excepting the Pine Barrens,-and, occasionally extending 
somewhat above the Fall-line. Ranges from Massachusetts 
to Florida and Texas. 


9. HemiantTuus Nutt. in Journ. Acad. Nat. Sci. Phila. 1: 119. 
1817. 
Type species, H. micranthemoides Nutt. 
1. Hemianthus micranthus (Pursh) Pennell, comb. nov. 
Herpestis micrantha Pursh, Fl. Am. Sept. 2: 418. 1814. 
‘On the banks of rivers, at the edge of low water mark: 
Pennsylvania to Virginia.”” Described as with five- 
leaved calyx, but no other plant can possibly be intended. 
Hemianthus micranthemoides Nutt. in Journ. Acad. Nat. 
Sei. Phila. x: 119. pl. 6. 1817: “Habitat fonmegme 
gravelly banks of the Delaware, overflowed by the tide, 
near Kensington [Pennsylvania].’”’ Type seen in the 
herbarium of the Academy of Natural Sciences. 
Micranthemum micranthum (Pursh) Wood, Class-Book 525. 


1861. 
Micranthemum Nuttalla A. Gray, Man. Bot. N. Un. St. ed. 
V. 331. 41867. ‘‘Hemianthus micranthemoides Nutt. 


.. . Tidal muddy banks of the Delaware River, and 
southward.” Typified by plant of Nuttall. 
Micranthemum nucranthemoides (Nutt.) Wettst. in Engl. & 
Prantl, Natiir. Pflanzenfam. 4°°:77. 1891. 
Globifera micranthemoides (Nutt.) Kuntze, Rev. Gen. 461. 
1891. 
Flowering from early September to October, and soon ripening 
fruit. 
Gravelly or sandy river-shores, between high and low tides, 


151 


Delaware and Chesapeake drainage, Along the Delaware 
River in New Jersey, Pennsylvania and Delaware. Also along 
the Potomac River in Virginia. 


10. LinARIA Mill. Gard. Dict. ed. IV. 1754 
Type species, Antirrhinum Linaria L. of Europe. 


Corolla, excluding spur, 15-18 mm. long, yellow; posterior lip 
arched over anterior; anterior lip forming a conspicuous pro- 
truding orange palate; spur tapering from a broad stout base. 
Capsule 10 mm. long, much exceeding the sepals. Style 8 
mm. long. Seeds 1.7 mm. long, flattened and circularly 
broadly-winged. Stem 3-10 dm. tall, densely leafy; without 
sterile prostrate branches from the base. 
(Linaria, sensu strictu.) 1. L. Linaria. 
Corolla, excluding spur, 7-8 mm. long, blue; posterior lip erect; 
anterior lip broadly spreading, but not forming a definite 
raised palate; spur very slender throughout. Capsule 2 mm. 
long, equaling to slightly exceeding the sepals. Style .8 mm. 
long. Seeds .3-.4 mm. long, cylindric, prismatic-angled, 
not winged. Stem very slender, 2-8 dm. tall, less leafy; with 
sterile prostrate branches from base. . 
(Leptoplectron, sect. nov.) 2. L. canadensis. 
1. LINARIA LINARIA (L.) Karst. 
Linaria pensylvanica Scheele in Flora 26: 586. 1843. ‘‘Aus 
Pensylvanien.”” Described as differing from L. vulgaris 
( = L. Linaria) by having the raceme axis and pedicels 
quite smooth instead of glandular-pubescent. JL. Linaria 
varies freely between these two states. 
Loam or sandy soil, fields and waste ground, common above the 
Fall-line, less common through the Coastal Plain. Naturalized 


from Eurasia. 


2. LINARIA CANADENSIS (L.) Dum.-Cours. 

Antirrhinum canadense L. Sp. Pl. 618. 1753. ‘Habitat in 
Virginia, Canada.’ Specimen in Linnean herbarium cred- 
ited to Canada should be the type. Thisis probablya plant 
collected by Kalm, and as Kalm spent much time near 
Philadelphia, especially on Raccoon Creek, Gloucester 
Co., New Jersey, in a district where this plant is very 
common, his specimen is probably from there. In Kalm’s 
Travels I: 358. 1770, this species is mentioned as if 


152 


common at Raccoon. Moreover it is a plant of rare 
occurrence and obviously recent introduction inany part 
of Canada. 

Linaria canadensis Dum.-Cours. Bot. Cult. 2: 96. 1802. 
“Lieu. Le Canada, la Virginie.” Doubtless based upon 
Antirrhinum canadense L. 

lowering from late April to October, and soon ripening 

fruit. 

Open sandy potassic soil, frequently a weed; thoughout the 
Coastal Plain of Long Island and New Jersey, but likely intro- 
duced into the Pine Barrens; above the Fall-line occasionally 
introduced along railroad-tracks. Ranges from Massachusetts 
to Florida and Texas.* 

(To be gontiamed.) 


REMINISCENCES OF ORCHID-HUNTING 


By HERBERT M. DENSLOW 


- 


One who has much to do with orchids garners a store of happy 
memories. The writer’s acquaintance with this fascinating 
family began in the year 1867 and extends over a period very 
nearly the same as the life of the Torrey Club. These recollec- 
tions, however, do not really cover this half century, but are 
concerned chiefly with about a dozen years at the beginning of it 
-and as many more since the year 1905. The interval was too 
much occupied with professional duties to leave more than 
occasional scraps of time for any hobbies. They were not barren 
years, for they included some fascinating excursions and thrilling 
discoveries; but they are not so crowded, in retrospect, with 
memories of orchid-hunting as are the earlier and the later periods. 

The earliest picture is of an extensive cranberry bog, long 
since drained and cultivated, in East Haven, Connecticut, in 
which on one unforgettable summer day, the novice, who had 


* The following plants are to be considered as scarcely established. 

CYMBALARIA CYMBALARIA (L.) Wettst., from Eurasia, is occasional along roadsides, 
and elsewhere near old gardens. 

KickxIA ELATINE (L.) Dumort. and K. spurta (L.) Dumort., both from Eurasia, 
are occasionally seen, mostly on ballast. 


153 


never seen even one orchid before, was introduced to three most 
attractive species, Pogonia ophioglossoides, Calopogon pulchellus 
and Habenaria ciliaris. There were other interesting plants in 
that bog, but no Vaccinium nor Andromeda nor Cassandra, nor 
all the rest, made any impression, in comparison with the orchids, 
all of which were in great profusion and in perfect bloom. From 
that day the writer dates the incomparable joys of orchid-study 
in field and forest and bog, and in books and conversations, 
during more than fifty years. There were many botanizing 
excursions near New Haven during the next few years, but no 
memories are particularly vivid, except those of collecting 
Arethusa in abundance, including one plant that bore two scapes 
and three flowers, in a bog that is now dry land, and of finding 
an occasional plant of Jsotria verticillata in fruit, never one in 
flower, in the woods adjacent to Edgewood, the home of Ik 
Marvel. 

On the upper end of Manhattan Island there were native 
orchids in those days. Ina bank by the side of a private road 
leading up through the woods from the New York Central Sta- 
tion at Inwood, was a small colony of Tipularia. Between that 
spot and “‘the Kingsbridge Road,’’ were found occasionally 
Liparis liliifolia, Goodyera pubescens, Corallorrhiza odontorhiza, 
Spiranthes gracilis and Spiranthes cernua; authentic specimens 
of which are preserved in the local herbarium of the New York 
Botanical Garden. The writing of these names reminds one of 
the changes in nomenclature, as well as in the region, since those 
earlier days; but these binomials are adequate for identification. 

Most of the writer’s orchid-hunting in recent years has been 
done in the town of Fairlee, Orange County, Vermont, where 
within about two square miles thirty-three species have been 
found, nearly one half of those listed in Gray’s Manual. This 
sutprising result began just ten years ago with the finding of 
Cypripedium arietinum in a most unexpected place. There 
hadn’t been any search for it; the writer was scrambling up a 
steep mountain, and there, on a dry slope, appeared this rara avis. 
The books report it as growing in bogs. It does; but it thrives 
on this stony declivity, where the slope is from 45° to 60°, where 


154 


the ground is dry almost at once after rain. It is restricted to 
an area of a few square rods, at an elevation of about 1000 feet. 
There are more than two hundred plants. They grow chiefly 
in groups of from three to six, and multiply apparently by 
.seed, which falls straight or is scattered a few feet by wind. 
This year scores of plants blossomed and nearly every blossom 
was fertilized, promptly; the anthesis is not longer than ten 
days. Evidently this orchid can get along with very little 
water. If we knew more about some species we should hesitate 
to indicate for them any restricted environment; and we should 
know more about them and less often call them ‘‘rare,” if we 
could go oftener to the secluded spots in which they delight to 
live. 

The most frequent orchid in Fairlee is Habenaria Hookeri. 
It is found on every wooded hill, sometimes even on roadside 
banks. In one morning’s ramble of three hours up and down on 
a small mountain, two hundred and seventeen plants of this 
species were counted, of which about one seventh were blossom- 
ing. HH. orbiculata grows in the same woods. It is less frequent 
and is now being exterminated by the logging that is stripping 
the hillside. Of these two related species, H. orbiculata seems 
to prefer to grow on a slope, H. Hookeri, in more level or sunken 
spots. The size of the leaves at anthesis, is no indication of the 
species; even H. macrophylla sometimes has leaves smaller than 
are found on some plants of H. Hookeri. Where H. orbiculata is 
fairly abundant, as it was on that now denuded hillside, it is a 
fine sight to look up the slope and see the many tall scapes with 
their striking flowers. This species is more readily discerned at 
a distance than H. Hookeri, not only because it is taller, but 
because it generally grows in more open spots. H. macrophylla 
is much rarer; though, in the summer of the year 1918, near 
St. Johnsbury, Vermont, it was found oftener than H. obiculata. 
Perhaps these are not specifically distinct. 

The latest species to be discovered, of the thirty-three now 
known in Fairlee, are the two northen Listeras, L. convallarioides 
and L. cordata, the former flourishing in a high, open swamp, the 
other, dying out, quite in contrast to its appearance on Mt. 


155 


Killington, thirty-six years ago, where, in a mossy belt that 
encircles the peak at an elevation of 3,500 feet, it was as frequent 
and as strongly intrenched as dandelions on a lawn. 

The pleasures of recent discovery have not all been experienced 
in Fairlee. They include the sudden view of a sunny hillside in 
open woods, in Albemarle County, Virginia, fairly studded with 
prosperous plants of Liparis liliifolia; the finding of Orchis 
spectabilis in the same woods in bloom on April 30 and of [sotria 
verticillata not far away, almost in a farm yard, a week later; 
the meeting of Cypripedium arietinum as frequently as H. 
Hookeri, in dry woods again, and even on exposed rocks, in 
Essex County, New York; and the much prized opportunity of 
studying A plectrum during one whole summer, from the wither- 
ing and decay of the old leaves until the appearing in early 
September of the reddish-brown tips of the next winter’s foliage. 
This plant is perhaps local rather than rare. Its peculiar habit 
helps to hide it. For three months, the months in which the 
collector is most busy, one could walk over the temporary graves 
of this abnormal species without suspicion of its nearness, un- 
less there had been a flowering scape and some of its ovaries had 
become fertile. These exceptions are infrequent; for only a 
small percentage of the bulbs send up scapes and, if these are 
not promptly visited by the proper insects, they shrivel and die 
within a few days. If, however, any one of the six to ten flowers 
on a scape is fertilized all are apt to share the benefit; and the 
strong stalks with their big capsules become conspicuous during 
the next summer or in the ensuing spring. Like many of the 
rarer orchids, A plectrum is more likely to be found by apparent 
chance than by search. 

For, orchid-hunting is an adventure always. It is impossible 
to predict that any species will be found in a certain locality or 
environment, however right and proper they may seem to be. 
Some lack or superfluity, in soil or surroundings, the crowding 
of some alien neighbors, the failure of a sheltering umbrage, the 
disappearance of some insect life may have caused extermina- 
tion; or the species may never have found the apparently favor- 
able habitat, where you seek for it in vain. The orchid-lover in 


156 


a new region is a true pioneer. Every step is an adventure, 
every moment pregnant with possibilities of delightful surprise. 
He may ramble or scramble for an hour without one cheering 
sight; when he pauses to take breath or to get his bearings, he 
may look down and see a Listera or some rarer Habenaria waiting 
to be admired. He may even hesitate to gather the treasure, 
for he knows thaz it will never present again an aspect so al- 
together charming as in its chosen place of growth. The col- 
lector of terrestrial orchids is bound to be something better than a 
hunter. In the tropics, gathering orchids may be chiefly com- 
mercial; in our zone, it is aesthetic in good part. The diligent 
searcher for these alluring denizens of meadow, bog and forest 
is not desirous simply to find herbarium specimens or to add to 
the number of local species; he enjoys the living plants, appre- 
ciates their oddities, is charmed by their almost bewildering 
variety of form and function, studies them in their homes, in 
their life. He enjoys the hunting, too, even when it is for the 
time unrewarded, for his search takes him into secluded places, © 
where the silence sometimes is “wide, velvety, complete”; 
where, with happier frequency, the solitude is vocal with the 
songs of birds or thrilling with the myriad, incessant, little noises 
of the wild; or his footsteps wander over a carpet of Linnaea or 
sink with cushiony comfort into fragrant beds of sphagnum; 
he tiptoes around or over quaking bogs and pauses to scrutinize 
tuft and tussock for an Arethusa or a Listera; while every moment 
he is pleasurably aware that his next glance may fall on some de- 
sired species that he has hunted for years or, with almost equal 
satisfaction, on one well-known, but beautiful, and not dises- 
teemed because familiar. Each orchid-lover who is able to 
roam the woods and fields and traverse the bogs finds in his 
own wishes and activities a perennial fountain of joy. While 
he is making new friends or renewing old acquaintance, he ‘is 
storing fragrant memories; many.a remote woodland spot be- 
comes as clear, to grateful recollection, as his own dwelling; he 
becomes too full perhaps of reminiscence, but never quite re- 
plete with adventure or ready to give over the search. 


FAIRLEE, 
VERMONT. 


PROCEEDINGS OF THE CLUB 
APRIL 30, I9I19 

The meeting was held in the Morphological Laboratory of the 
New York Botanical Garden. Vice-President Barnhart called 
the meeting to order at 3:30 P.M. There were fifteen persons 
present. 

The minutes of February 26, March 11, March 25 and April 
8 were read and approved. Mrs. Britton, Chairman of the 
Program Committee madea report. She also asked for authority 
to call a special meeting on Tuesday, May 15, at 3:30 P.M., to 
be held at the Mansion of the New York Botanical Garden in 
cooperation with the Wild Flower Preservation Society of 
America in order to organize a local chapter and have the Club 
become an associate member, as TORREYA has already been 
authorized as the organ of the Wild Flower Preservation Society. 
On motion of Professor Harper the Program Committee was in- 
structed to call a special meeting. 

Dr. Howe moved to instruct the Treasurer to donate to the 
University of Louvain through Columbia University such of 
the Club’s publications as are available. 

Mrs. Britton exhibited a plant of Sisyrhynchium bermudiana, 
grown at the New York Botanical Garden from a plant collected 
in Bermuda, and called attention to the fact that the color had 
a definite tone, much less blue than any of our native species. 

The announced scientific program consisted of a paper on 
“The Scrophulariaceae of the Local Flora,’’ by Dr. F. W. Pen- 
nell. An abstract furnished by the speaker follows: 

An account was given of the species of Scrophulariaceae occur- 
ring within the local flora range of the Torrey and of the Philadel- 
phia Botanical Clubs. Comment was made of specific characteris- 
tics and of distribution. Within this area there are native: 40 
species belonging to 19 genera; introduced: 24 species belonging 
to 7 genera—in all 64 species and 22 genera. 

A key proposing a more evolutionary sequence of genera was 
here first presented. This with a summary of the species it 
is proposed to publish in forthcoming numbers of TORREYA. 
Specimens were shown illustrating all species of the area. 


| 158 


May 13, 1919 

The Club met at the American Museum of Natural History. 
President Richards called the meeting to order at 8:15 P.M. 
There were twenty persons present. 

Dr. F. W. Pennell, chairman of the Field Committee, dis- 
cussed the proposal to announce a joint field excursion with the 
Philadelphia Botanical Club to Farmingdale, N. J., on May 
30. He proposed to make the excursion a one-day trip with 
the provision that anyone wishing to stay over could do so. 
The motion to adopt this suggestion was carried. 

President Richards announced that the goth birthday of 
Capt. J. Donnell Smith would occur in the near future. Dr. 
Pennell moved to appoint a committee to write a letter of felici- 
tation to Capt. Smith, expressing the Club’s appreciation of 
the memorable work he has done in advancing the knowledge of 
plants. The President appointed Dr. N. L. Britton, Dr. R. A. 
Harper and Dr. M. A. Howe, members of the committee to draw 
up this letter. 

No other business was transacted. 

Dr. Isaac Levin gave the lecture of the evening, ‘‘ Neoplastic 
Diseases (Cancer) in the Animal and vegetable Kingdoms.” 
The lecture was illustrated by lantern slides. 


Adjournment followed. 
B. ©: Dopes 


Secretary. 
NEWS ITEMS 


Dr. D. S. Johnson of Johns Hopkins University, accompanied 
by three of his students, has just returned from Jamaica. Col- 
lections for morphological work were made in the Blue Moun- 
tain region and in Liguanea Plains. 


W. H. Blanchard wishes his botanical friends and correspond- 
ents to know that, owing to the development of cataracts on 
both eyes, his botanical work seems at an end. Mr. Blanchard 
was a frequent contributor to the American botanical press from 
1902 to 1911, most of his published work relating to the genus 
Rubus as it occurs in eastern North America; his summary of 


159 


his conclusions regarding the species of this genus in that area 
was published in the Bulletin of the Torrey Botanical Club (38: 


425-439. I91I.) 


Messrs. Barrington Moore, G. P. Burns, C. C. Adams, T. P. 
Hankinson and Norman Taylor, spent a week in August study- 
ing the ecological relations of the plants and animals near the 
summit of Mt. Marcy in the Adirondacks. This trip was to 
continue work started during the first week in June by the com- 
mittee on cooperation of the Ecological Society in America. 


One of the most dangerous diseases of Irish potatoes has been 
discovered in the United States. Rough, spongy outgrowths of 
varying size are produced on the tubers, especially at the eyes. 
These warts are light brown at first, but become black and 
decayed with age. Sometimes all potatoes in affected hills are 
worthless. The disease does not attack the vines above ground. 
The wart is caused by a parasitic fungus (Chrysophlyctis endo- 
biotica Schilb.), which was named and described by Schilberszky, 
a Hungarian scientist, in 1896. It is one of the lowest members 
of the Chytridiaceae, a group of parasites that attack the stems, 
leaves, and especially the roots of many wild and cultivated 
plants. Although it belongs in the same great group of fungi 
as the common bread mold, it produces no mold growth and is 
so small that it can hardly be seen with the naked eye. 


The first volume of The Cactaceae by N. L. Britton and J. N. 
Rose was issued by the Carnegie Institution on June 21. The 
work will comprise four volumes. The first contains descrip- 
tions and illustrations of groups allied to Opuntia and of the 
prickly pears themselves, and is one of the most sumptuous 
botanical publications recently issued. It will be reviewed in 
an early issue of TORREYA. . 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of TorREYA in which their papers appear, will kindly notify the 
editor when returning proof. 

Reprints should be ordered, when galley proof is returned to the editor. The 
New.Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
following rates: 


2pp 4pp 8pp 12pp 16pp 20pp 
25 copies $ .79 $1.14 $1.78 $2.32 $2.87 $3.28 
50 copies 1.03 1.43 2.23 2.82 3.52 3.92 
100 copies 1.45 2.03 2.73 3.50 4.23 4.55 
200 copies 2.15 3.24 3.92 525 6.52 6.92 


Covers: 25 for $1.00, additional covers 114 cents each. 
Plates for reprints, 50 cents each per 100. 


Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs. E. G. BRITTON, Chairman. 
J. H. BARNHART, Pror. JEAN BROADHURST 
Miss C. C. HAYNES B. O. DopGE 
SERENO STETSON MICHAEL LEVINE 
Budget Committee F. J. SEAVER 
J. H. BARNHART, Chairman. Membership Committee 
R. A. HARPER J. K. SMALL, Chairman. 
N. L. BRITTON T. E. HAZEN 
A. W. Evans E. W. OLIVE 
M. A. Howe Local Flora Committee 
H. H. Russy N. L. Britton, Chairman. 
Field Committee Phanerogams: Cryptogams: 
F. W. PENNELL, Chairman. E. P. BICKNELL Mrs. E.G. BRITTCN 
Mrs. L. M. KEELER N. L. BRITTON T. E. Hazen 
MICHAEL LEVINE C. C. CurRTIS M. A. Howe 
GEORGE T. HASTINGS K. K. MACKENZIE MICHAEL LEVINE 
PERCY WILSON : NORMAN TAYLOR W. A. MurRRILL 


F. J. SEAVER 
Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M. Richards, F. 
Except Russula and Lactarius: MissG: ~ Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurs 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


OTHER PUBLICATIONS 


OF THE > 


TORREY BOTANICAL CLUB 


(1) BULLETIN 


A monthly journal devoted to general botany, established 
#870. Vol. 45 published in 1918, contained 519 pages of text 
and 15 full-page plates. Price $4.00 per annum. For Europe, 
18 shillings. Dulau & Co., 47 Soho Square, London, are, 
agents for England. 

Of former volumes, only 24-45 can be supplied entire ; cer- 


tain numbers of other volumes are available, but the entire stock - 


of some numbers has been reserved for the completion of sets 
Vols. 24-27 are furnished at the published price of two dollars 
each; Vols. 28-45 three dollars each. 

Single copies (30 cents) will be furnished only when not 
breaking complete volumes. 


(2) MEMOIRS 


The Mewnoirs, established 1889, are published at irregu- 
lar intervals. Volumes I-15 are now completed ;-No. 1 of 
Vol. 16 has been issued. The subscription price is fixed at 
$3.00 per volume in advance; Vol. 17, containing Proceedings 
of the Semi-Centennial Anniversary of the Club, 490 pages, was 
issued in 1918, price $5.00. Certain numbers can also be: pur- 
chased singly. A list of titles of the individual papers and of 
prices will be furnished on application. 


(3) The Preliminary Catalogue of Anthophyta and Pteri- 
dophyta reported as growing within one hundred, miles of New 
York, 1888. Price, $1.00. 


Correspondence relating to the above publications should be 
addressed to 
DR. BERNARD O. DODGE 
Columbia University 


New York City 


Vol. 19 September, Ig919 No. 9 


PORKEY A © 


A MonTuiy Journat or BoranicaL Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873. 


% CONTENTS 
Scrophulariaceae of the Local Flora, III: F. W. PENNELL «0.0.40. -0c0e eee eeeseeee ene 161 
A. New Cuban Sida < BROTHER: LEON: (2s cae doc dae see suk o's dn pau op dened qVcsbhnrens (U0 es pebea- 172 


Flora of Southern British Columbia and the State of Washington: J. C. NELSON 174 


News Items... ... .... -.. Sisson igh were dad EN aew s Woe Atl takes Ga! tpn Sa Pe se neal eee p sa Ran: 185 


PUBLISHED FOR THE CLUB 


At 41 NortH Queen Street, Lancaster, Pa. 
BY Tur New ERA Printinc Company 
“Entered at the Post Office at Lancaster, Pa., as second-class matter. 


THE TORREY BOTANICAL CLUB 


OFFICERS FOR 1019 


President 
H. M. RICHARDS, Sc.D. 


Vice-Presidents. 
JOHN HENDLEY BARNHART, A.M., M.D 
C. STUART GAGER, Pu.D. 


Secretary and Treasurer 
BERNARD O. DODGE, Pu.D. 
COLUMBIA UNIVERSITY, N. Y. City. 
Editor 
ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


JEAN BROADHURST, Puz.D. M. LEVINE, Pu.D. 
. J. A. HARRIS, Pu.D. . E. NICHOLS, Px.D. 
MARSHALL AVERY HOWE, Pu.D. ARLOW B. STOUT, PH.D. 


NORMAN. TAYLOR. 


Delegate to the Council of the New York Academy of Sciences 
M. A. HOWE, PH.D. 


OFFICIAL ORGAN OF THE WILD FLOWER PRESERVATION 
SOCIETY OF AMERICA 


TorRREYA is furnished to subscribers in the United States and 
Canada for one dollar per annum; single copies, fifteen cents. To 
subscribers elsewhere, five shillings, or the equivalent thereof. Postal or 
express money orders and drafts or personal checks on New York City 
banks are accepted in payment, but the rules of the New York Clearing — 
House compel the request that ten cents be added to the amount of any 
other local checks that may be sent. Subscriptions are received only* 
for full volumes, beginning with the January issue. Reprints will be 
furnished at cost prices. Subscriptions and remittances should be sent” 
to TREASURER, TORREY BOTANICAL CLusB, 41 North Queen St., Lan- 
caster, Pa., or Columbia University, New York City. 

Matter for publication, and books and papers for review, should 
be addressed to 


NORMAN TAYLOR 
Brooklyn Botanic Garden 
Brooklyn, N. Y 


wa 


- 


TORREYA 


Vol. Ig No. 9 
September, IgIg 


SCROPHULARIACEAE OF THE LOCAL FLORA. III 


By FRANCIS W. PENNELL 


(Continued from August TORREYA) 


II. VERONICASTRUM Heister; Fabr. Enum. meth. pl. Hort. 
Helmstead. III. 1759 
Type species, Veronica virginica L. 
1. VERONICASTRUM VIRGINICUM (L.) Farwell. 
ginia.”” Grown in the Clifford-garden. 
Veronicastrum album Moench, Meth. 437. 1794. “ 
Le Ae Veronica virginica L.” 
Calistachya alba Raf. in Med. Repos. N. Y. II. Hex. 
5: 352. 1808. 
Based on Veronica virginica L. Type of Calistachya 
Raf., not Callistachys Vent., 1804. 
Leptandra virginica (L.) Nutt. Gen. N. Am. Pl. 1:7. 1818. 
Type of Leptandra Nutt. 
Eustachya alba (Raf.) Raf., Cat. 14. -1824. Eustachya 
Raf. in Am. Mo. Mag. 4: I90. 1819, was a new name 
for Calistachya Raf. Preoccupied by Eustachys Desv., 


1810. 
Leptandra alba Raf. Med. Fl. 2: 21. 1830. ‘The true 
Vs vt einicd ob, no, ae ee The most common species 


being found all over the United States.”’ 
Paederota virginica (L.) Torr., Fl. N. Y. 2:44. 1843. 
Calistachya virginica (L.) Farwell in Mich. Acad. Sci. Rep. 
£7; 176.8 -103 5. 
Veronicastrum virginicum (L.) Farwell, Drugg. Circ. 61: 
23%; SOEs 
[No. 8, Vol. 19, of TORREYA, comprising pp. 143-159, was issued Sept. 17, 1919] 


161 


162 


Varying, in number of leaves in whorl (five, reducing to four 
or three), in inflorescence of one or several racemes, and in 
leaves from lanceolate to nearly ovate, pubescent to nearly or 
quite glabrous beneath. 

Flowering from mid-July to early September, and soon ripen- 
ing fruit. 

Sandy or loam soil, swales and moist meadows, in potassic, 
magnesian and calcareous soils, frequent above the Fall-line; 
in western Long Island, and occasional in Middle district of 
New Jersey. Ranges from Connecticut and Ontario to Missis- 
sippi, Minnesota and Texas. 


VERONICAUE Sp blon 1753 
Type species, Veronica officinalis L., of Europe. 


Flowers solitary, axillary, frequently approximating 
so as to form a terminal raceme. Leaves alter- 
nate through the inflorescence. 

Filaments not exceeding the lobes of the corolla. 
Bracts leaf-like or slightly reduced. Plants 
less than 3 dm. tall. 

Pedicels longer than the sepals, usually exceed- 
ing the bracts. Sepals ovate. Capsule 
turgid. Seeds few, 1.3-3 mm. long, con- 
vex-arched, roughened. Leaves petioled 
(rarely the uppermost sessile), primarily 
palmately 5-7 nerved, the midvein 
usually with some radiating pinnate 
veins; mainly alternate, the lower some- 
times opposite. : i 

Leaves broadly cordate, 3-5 lobed, the 
lobes rounded. Sepals broadly ovate, 
conspicuously ciliate. Capsule very 
turgid, scarcely notched at apex, only 
slightly 2-lobed. Seeds 2.5-3 mm. long, 
blackish. 1. V. hederaefolia. 
Leaves ovate, serrate to dentate. Sepals : 
more shortly ciliate. Capsule slightly 
flattened, deeply notched at apex, thus 
strongly two-lobed. Seeds 1.3-1.5 
mm. long, brown. 

Petals not exceeding the ovate sepals. 
Capsule-lobes rounded, the most 
distal point of each about midway 
between the style and the lateral 
margin. 2. VY. agrestis. 


163 


Petals exceeding. the narrowly ovate 
sepals. Capsule-lobes acutish, the 
most distal point of each near the 
lateral margin. 

Pedicels shorter than sepals or bracts. Sepals 
linear to narrowly ovate. Capsules 
flattened. Seeds many, less than I mm. 
long, flat, smooth or nearly so. Leaves 
sessile (or the lower petioled), scarcely 
palmate; alternate only through the 
inflorescence. 

Perennials. Repent, with ascending stems. 
Leaves oval or ovate, obscurely cre- 
nate. Inflorescence spike-like, re- 
stricted to the distal portion of the 
stem. Sepals ovate. Corolla blue 
or white, with deep-blue lines on 
posterior side. Capsule retuse or 
shallowly notched, glandular-pubes- 
cent. 

Leaves prevailingly oval. Stems dis- 
tally and pedicels minutely pubescent 
with appressed hairs. Corolla 2 mm. 
long, white, with blue lines on pos- 
terior side. 

Leaves prevailingly ovate. Stems dis- 
tally and pedicels finely pubescent 
with mostly spreading hairs. Corolla 
3 mm. long, blue on posterior side, 
anterior lobe nearly white; with deep- 
blue lines on posterior side. 

Annuals. Erect, much branched below. 
Most leaf-axils flower-bearing. Se- 
pals lanceolate to linear. Capsule 
deeply notched. 

Lower stem-leaves ovate, crenate-ser- 
rate, the lowermost frequently pet- 
ioled. Corolla deep violet-blue. 
Capsule pubescent with slightly 
gland-tipped hairs. Plant pubescent 
with glandless hairs. 

Lower stem-leaves oblanceolate, entire 
or distally remotely toothed, all 
sessile. Corolla whitish through- 
out. Capsule glabrous. Plant 
glabrous or with short gland- 
tipped hairs. 

Stem glabrous. 


3. V. Tournefortii. 


4. V. serpyllifolia. 


5. V. ruderalis. 


6. V. arvensis. 


7. V. peregrina. 


164 


Stem pubescent witlt gland-tipped 
hairs. 7a. V. peregrina xalapensis. 
Filaments much exceeding the lobes of the corolla. 
Bracts linear, abruptly reduced from the lanceo- 
late foliage-leaves. Plants 6-10 dm. tall. 
Perennial. 8. V. longifolia. 
Flowers all in axillary small-bracted racemes. Leaves 
opposite throughout. Perennials. 
Stem, pedicels, leaves and sepals pubescent. -Cap- 
sules pubescent. Leaves oval or ovate, 
serrate to dentate. Plants of dry soil. 
Leaves sessile or nearly so, ovate, dentate, the 
largest cordate at base. Sepals 4-5 mm. 
long, linear-lanceolate, exceeding the 
capsule. Capsule not glandular, its 
lobes broadly rounded. Ascending or 
erect. 
Stem erect, 3-5 dm. tall. Leaves coarsely 
dentate. Racemes 30-60 flowered, the 
pedicels scarcely exceeding the bracts. 
Largest corolla-lobes ovate, 6 mm. long, 
violet. 9. V. Teucrium. 
Stem ascending, I-3 dm. tall. Leaves 
crenately dentate. Racemes 10-20 
flowered, the pedicels much exceeding 
their bracts. Largest corolla-lobes 
nearly orbicular, 3.5—4 mm. long, violet- 
blue. to. V. Chamaedrys. 
Leaves oval, crenate-serrate, narrowed to a 
petiolar base. Sepals 2-3 mm. long, lanceo- 
late, shorter than the capsule. Capsule 
glandular, the most distal point being near 
the lateral margin of each lobe. Exten- 
sively repent, at apex ascending. It. V. officinalis. 
Stem, pedicels, leaves and cepals glabrous (or in 
V. glandifera slightly pubescent with gland- 
tipped hairs). Capsules glabrous. Leaves 
oblong-ovate to linear, obscurely crenate- 
serrate to entire. Aquatics. 
Capsule scarcely or not wider than long, and 
scarcely or not two-lobed. Sepals equal- 
ing the capsule. Leaves oblong-ovate to 
broadly lanceolate, obscurely crenate- 
serrate. 
Leaves all petioled. Racemes usually ro- 
25 flowered. Plant emersed. 12. V. americana. 
Leaves sessile and clasping (or only the 
upper or lowermost petioled). Ra- 


165 


cemes usually longer, 25—50 flowered. 
In deeper water, usually mostly sub- 
mersed. 
Stem distally, rachis and pedicels gla- 
brous. Leaves oblong-ovate, mostly 
broadest about the middle, the low- 
est, especially if submersed, narrow- 
ing to a petiolar base. Capsule 
globose-ovoid, not or scarcely emar- 
ginate. 13. V. Brittonii. 
Stem distally, rachis and _ pedicels 
sparsely pubescent with glands, borne 
upon jointed stalks. Leaves lanceo- 
late, broadest near the base, the low- 
est submersed ones elongated-lanceo- 
late, clasping. Capsule broad-glo- 
bose, emarginate. 14. V. glandifera. 
Capsule much wider than long, strongly two- 
lobed. Sepals shorter than the capsule. 
Leaves linear or nearly so, remotely setace- 
5. V. scutellata. 


e 
1 


ous-toothed to entire. 


I. VERONICA HEDERAEFOLIA L. 
Occasionally introduced into waste ands, mostly near cities. 
From Eurasia. 


2. VERONICA AGRESTIS L. 
Occasionally introduced into waste land, mostly near cities. 
From Eurasia. 


3. VERONICA TOURNEFORTII C. C. Gmel. 

Veronica precox Raf. Atl. Journ. 79. 1832. ‘‘Grown in 
the [Bartram’s Botanic] Garden [near Philadelphia] 
from seeds received from a place unknown; but has spread 
all over the garden like a weed, and even is become spon- 
taneous on the banks of the Schuylkill.’”’ Not V. praecox 


All., 1789. 
Veronica diffusa Raf., New Fl. Am. 4: 38. 1838. “Native 
of ——— naturalized on the Schuylkill near Philadel- 


phia.”” Re-naming of V. precox Raf. 
Occasionally introduced into waste land. From Eurasia. 
4. VERONICA SERPYLLIFOLIA L. 
Common in moist grassy soil, meadows, fields and lawns. 
From Eurasia. 


166 


5. VERONICA RUDERALIS Vahl, Enum. Pl.1:66. 1805. ‘‘Habi- 
tat in ruderatis versuris et humidis locis frigidis Peruviae.”’ 
Type not seen nor verified, but specimens from Ecuador 
and those collected by the writer in Colombia show the 
identity of this with the plant here considered. 

This is the plant identified in the seventh edition of Grays 
Manual as Veronica humifusa Dickson. This species, published 
in Trans. Linn. Soc. 2: 288. 1794, and found by James Dickson 
on ‘‘very high mountains of Scotland,’’ was described by him 
as a plant wholly prostrate, with cordate-subrotund minutely 
scabrous leaves which often occur in threes or fours, and with 
a short raceme of a few crowded flowers. Whatever this may 
be, it surely cannot be our plant. 

Veronica ruderalis appears to be the most cosmopolitan species 
of the genus, and doubtless V. serpyllifolia must be considered 
as a Palaearctic derivative from it. It is a boreal or mountain 
species through Eurasia and the Americas. One European 
description which I have had no opportunity to see, that of 
Veronica neglecta F. W. Schmidt, Fl. Boem. 1: 12. 1794, may 
give a name which possibly must supersede ours. This is identi- 
fied by Koch, Syn. Fl. Germ. & Helv. 529. 1837, as a larger 
ovate-leaved form of V. serpyllifolia. However in the fifth 
(Hallier’s) edition of the Flora von Deutschland of Schlechten- 
dahl and Others, 17: 150, while this is similarly characterized, 
the glandular-pubescent plant is distinguished as var. borealis 
Laestad. So it would appear safer to consider neglecta as but 
a robust state of the appressed-pubescent serpyllifolia. 

I agree with Prof. Fernald, in Rhodora 4: 194. 1902, that 
“the evidence at hand indicates that this large-flowered variety 
is the only indigenous form of V. serpyllifolia in Northeastern 
America.” I follow his later judgment as expressed in the Grays 
New Manual, and in Rhodora 13: 124. I9gII, in according this 
specific rank. However I see no basis for the decision of the 
new Gray that serpyllifolia is likewise indigenous. Its occur- 
rence in North America is south of the region normally occupied 
by species common to both this continent and Europe. 

Apparently this has been collected in our range by C. F. 


167 


Austin in Sullivan Co., New York in 1860. It was labeled by 


” 


him “large form. 
6. VERONICA ARVENSIS L. 
Common in cultivated soil. From Eurasia. 

7. VERONICA PEREGRINA L. Sp. Pl. 14. 1753. ‘‘Habitat in 
Europae hortis, arvisque.’’ Described, as the specific name 
would suggest, from specimens of an introduced plant. 

Certainly American in origin, but it is difficult or impossible 
to say of what portion of this hemisphere it is indigenous. An 
abundant weed in moist cultivated soil. 

za. Veronica peregrina xalapensis (H. B. K.) Pennell, comb. 


nov. 

Veronica xalapensis H. B. K., Nov. Gen. et Sp. 2: 389. 
1817. “‘Crescit in Regno Mexicano prope Xalapa 
(alt. 630 hex.), in nemoribus Liquidambaris Styraci- 
fluae.”’ 


Occasional in cultivated soil. In the western half of the conti- 
nent this glandular-pubescent plant completely replaces true 
peregrina. In the east it is only occasionally seen, and that 
probably as an introduction. Intergradation to the species 
seems to be complete. 

8. VERONICA LONGIFOLIA L. 
Rare in waste land. From Eurasia. 
g. VERONICA TEUCRIUM L. 

Rare in grass or waste land. From Eurasia. 
10. VERONICA CHAMAEDRYS L. 

Occasional in grass land. From Eurasia. 
IL. VERONICA OFFICINALIS L. 

Common in pasture fields and waste lands. In colonial times 
this was grown as a medicinal plant, and very early became es- 
tablished as if native. From Eurasia. 

12. VERONICA AMERICANA Schwein. 
Veronica Beccabunga americana Raf., Med. Fl. 2: tog. 
1830. ‘It grows from Canada to Virginia and Kentucky, 
near water, brooks, &c.” 
Veronica americana Schwein.; Benth. in DC., Prod. 10: 
468. 1846. “Veronica americana (Schweinitz! mss.) 


168 


In America boreali a Canada et Carolina usque 
ad flum. Oregon et in ins. Sitcha-- - (v.s.)’’ Speci- 
men seen in herbarium of the Academy of Natural Sci- 
ences of Philadelphia, labeled ‘“Bethl.’’ [Bethlehem, 
Pennsylvania], collected by Schweinitz, may be of collec- 
tion seen by Bentham. 

Flowering from late May to mid-August, and soon ripening 
fruit. 

Springheads in woodland, and along cool streams, in potassic 
soil, frequent throughout the area above the Fall-line; in nor- 
thern and westernmost Long Island. Ranges from Quebec to 
Alaska, south to South Carolina, New Mexico and California. 


13. Veronica Brittonii PORTER sp. nov. 

Veronica Anagallis latifolia Britton in Bull. Torr. Bot. 
Club 12:49. 1885. “In the latter part of September 
1883, - - - near Mahwah, Bergen Co., New Jersey, I 
noticed [this] in a small stream which crosses the N. Y. 
L. E. & W. R. R., half a mile or so north of the station.” 
Type seen in herbarium of Columbia University at the 
New York Botanical Garden. 

Stem 3-9 dm. long, glabrous, succulent, hollow. Leaves 
oblong-ovate to oval, acute, crenate-serrate to nearly entire, 
5-10 cm. long, 3-5 cm. wide, clasping, the lowest narrowed to 
a petiolar base. On autumnal shoots all the leaves are ovate 
and definitely petioled. Racemes axillary to the upper leaves, 
6-12 cm. long, 40-60 flowered. Bracts narrowly lanceolate, 
4-5 mm. long. Pedicels 3.5-4.5 mm. long, glabrous. Sepals 
3-3.5 mm. long, lance-ovate, acute. Corolla 4 mm. long, with 
a few hairs within throat, pale-blue, paler anteriorly, with longi- 
tudinal reddish-violet lines. Capsule 3-3.5 mm. long, globose- 
ovoid, acutish. Seeds .4 mm. long, oval, yellow-brown. 


Type, base of Marble Hill, above Phillipsburg, New Jersey, 
collected in flower and fruit June 24, 1892, 7. C. Porter; in her- 
barium Columbia University at the New York Botanical Garden. 
This specimen shows the summer state. Specimens collected 
at the same station October 9, 1892, show excellently the autum- 
nal condition. 

In the herbarium of Columbia University is a manuscript 


169 


description by Dr. Thomas C. Porter, the diagnosis of which 
includes such field knowledge as to make it worth quoting in 
full: ‘‘ VERONICA BRITTONIIL, n. sp. 

“(V. Anagallis L., var. latifolia Britton). Glabrous, perennial, 
growing in shallow, shaded rivulets: In its summer state (June), 
the stems are erect, simple or branching, 2 to 3 feet high, round, 
often half an inch in diameter, succulent, fistular, brittle; the 
leaves ovate or oblong-ovate, variable in size, 2 to 3 inches in 
length, more or less clasping at base, the lowest pair sometimes 
contracted into short petioles; racemes numerous, many-flowered. 
In its autumn-state (October), the stems are procumbent at 
base and rooting at the joints, rarely producing racemes of 
flowers; the leaves large, orbicular, 114 to 2 inches in diameter, 
abruptly narrowed into broadly margined petioles, % to an 
inch long, shining, thickish when fresh, with prominent veins 
beneath, thin when dried, crenulate, those of the slender branches 
similar but much smaller, petioles of the uppermost very short 
or wanting. Inflorescence, fruit and seeds scarcely to be dis- 
tinguished from those of V. Anagallis and V. Beccabunga; 
flowers pale blue, the three large lobes marked with reddish 
stripes; capsules orbiculate, acutish.’’ Then follow citation of 
specimens from northeastern Pennsylvania and northwestern 
New Jersey, and considerable interesting comment. 

From a series of letters of Dr. Porter to Dr. Britton, the 
history of the former’s interest in this plant may be traced. It 
commenced with finding on October 1, 1891 at Pot Rock, near 
Easton, Pennsylvania, a colony of the autumnal petioled-leaved 
form. On the 5th he wrote of having visited a colony of the 
plant in ‘‘the little run beside the tavern above Pot Rock,”’ 
-a station whence in “in midsummer two or three years ago”’ 
he had obtained ‘‘a very different form.’”’ The plant was abund- 
ant, and exactly that of the first discovery. On the 12th, Dr. 
Porter was “‘fully convinced that this plant is genuine V. Bec- 
cabunga, L.,”’ and accordingly sent a note for the Torrey Bulletin 
to urge this opinion. He had even convinced himself of its 
introduction from the Old World. But for us the most interest- 
ing paragraph of this note is that contrasting the autumnal 
state of this plant with Veronica americana: 


170 


“Veronica Americana Schwein., a nearly allied species, which 
has likewise petioled leaves, was growing with it in some places, 
but its procumbent, far less robust stems and its smaller, ovate 
or lance-ovate, sharply serrated leaves furnished a striking con- 
trast. In seeing them thus together even an unpracticed eye 
could not have failed to distinguish the one from the other. 
Intermediate forms were wholly wanting, so that the conjecture 
that it either must be an abnormal growth of that species, or 
a new variety is wide of the mark.” 

Flowering from late May to early October, and soon ripening 
fruit. ; 

“Shallow shaded rivulets,’”’ through Piedmont Region above 
the Fall-line, western Connecticut to Northeastern Pennsylvania; 
reported by Porter from Franklin County, Pennsylvania, and 
seen from Keweenaw County, Michigan, collected July 8, 
1915 by O. A. Farwell 4005. 

ConneEcTiIcuT.* Litchfield: North Canaan, #. B. Harger 
6238 (A). 

New York. Greene: New Baltimore, N. Taylor 1289 (Y). 
Queens: Flushing, J. A. Bisky (E, Y); Jamaica (Y). Rockland: 
Spring Valley (Y); Tappan, W. H. Leggett (Y). 

New JERSEY. Bergen: Carlstadt (Y); Carlton Hill, G. V. 
Nash 244 (Y); Mahwah (Y). Hunterdon: banks of Delaware 
River above Stockton, C. S. Williamson (A). Passaic: Passaic, 
E. W. Berry (Y). (P) Warren: Flatbrookville, (A); Manunka 
Chunk, Phillipsburg, T. C. Porter (A, Y). 

PENNSYLVANIA. Northampton: Pot Rock, etc., near Easton, 
T. C. Porter (A, P, Y); Johnsonville (A); Martins Creek (A); 
Riverton (A). 


14. Veronica glandifera Pennell sp. nov. 


Flowering stem 3-9 dm. long, glabrous or distally glandular- 
pubescent. Leaves lanceolate, acuminate, more or less serrate, 


* Localities for specimens seen are grouped by counties, and these listed in 
alphabetic sequence. 
Herbaria cited: A. Academy of Natural Sciences, Philadelphia. 
. Brooklyn Botanic Garden, Brooklyn. 
. University of Pennsylvania, Philadelphia. 
. New York Botanical Garden, New York. 


Kt 


171 


7-10 cm. long, 1.2-2.5 cm. wide, all clasping, the lowest sub- 
mersed ones elongated. Racemes axillary to the upper leaves, 
10-20 cm. long, 30-60 flowered. Bracts narrowly lanceolate, 
4-6 mm. long. Pedicels 3-6 mm. long, glandular-pubescent 
with scattered hairs. Sepals 3-4 mm. long, lanceolate, acute to 
acuminate. Corolla about 3 mm. long, not seen fresh. Cap- 
sule 2.5-3 mm. long, 3-3.5 mm. broad, broad-globose, emargi- 
nate. Seeds .4 mm. long, oval, yellow-brown. 


Type, vicinity of Suffolk, Nansemond County, Virginia, 
collected in flower and fruit May 27, 1893. N. L. Britton and 
J. K. Small: in herbarium Columbia University at the New York 
Botanical Garden. 

Flowering from late May to late July, and soon ripening 
fruit. 

Shallow flowing streams, mainly in calcareous soil, through the 
lower Piedmont from the Delaware valley southwestward.* 
Ranges from New Jersey to North Carolina, Minnesota and 
Kentucky. 

NEw Jersey. Warren: Warrenville, C. S. Williamson (P). 

PENNSYLVANIA. Bucks: Rockhill, A. MacElwee (A); Sellers- 
ville (A). CHESTER: West Chester, W. Darlington (A, Y). Lan- 
caster: Dillerville Swamp, J. K. Small (Y). Montgomery: 
Conshohocken (A); Manayunk, Shannonville J. Crawford (A) 
Philadelphia: East Park (P) J. C. Martindale (A). Wayne 
Junction (A). 

15. VERONICA SCUTELLATA L., Sp. Pl. 12. 1753. ‘“‘Habitat in 
Europae inundatis.”’ ; 

Flowering from late May to September, and soon ripening 
fruit. 

Swales and along streams, through the area above the Fall- 
line, becoming common northward. Ranges from Newfound- 
land to Yukon, south to Virginia, Wyoming and California; 
also through Eurasia. 

(To be continued) 

* In the herbarium of the Charleston Museum, Charleston, South Carolina, isa 
sheet of glandifera bearing the inscription ‘‘ Marlindicator!! Va. M.T.’’ Dr. Barn- 
hart identifies this comment as that of Michael Tuomey, a teacher in Virginia, who 


afterward became State Geologist of South Carolina, My only finding of this 
plant has been on limestone at Natural Bridge, Virginia, Pennell 9802. 


172 


A NEW CUBAN SIDA 


By BROTHER LEON 


Sida Brittoni Fr. Léon, sp. nov. 

Perennial; stems hirsute-strigose, diffusely branched at the 
base, prostrate, 3 to 4 dm. long, the branches ascending or pros- 
trate; leaves oblong to elliptic or obovate, rounded at apex, 
serrate above the middle, 1 to 2 cm. long, 4 to 9 mm. wide, 
subcordate at base, long-ciliate, hirsute on both surfaces, with 
long scattered stellate hairs beneath; petioles 4 to 7 mm. long; 
stipules linear or somewhat spatulate, long-ciliate, little longer 
than the petioles; flowers clustered at the end of the branches; 
pedicels shorter than the subtending petioles; calyx 5-lobed, 
5 mm. long, its lobes ovate, acute, long-ciliate, slightly longer 
than the tube, densely hirsute within; petals yellow, about 13 
mm. long, puberulent; style-branches 5, red, slender, 4 mm. 
long; carpels 5, 2.7 mm. long, puberulent, sharply reticulate- 
wrinkled, 2-pointed at apex, I-seeded, partially 2-valved; seed 
3-angled, 2 mm. long, brown, filling the cavity. 

Dry savanna, Chirigota, Pinar del Rio, Léon @ Roca 7466. 

This species was collected by the writer in company with 
Father Modesto Roca Masden, on August 9, 1917, in the savanna 
of Chirigota, near Santa Cruz de los Pinos, Pinar del Rio pro- 
vince.* This locality is well known to the botanists who have 
studied the flora of Cuba, a number of rare plants having been 
collected there by Charles Wright, who, for several years, had 
his quarters not very far away, at Retiro, at the foot of the 
western mountain range. 

North of the road which connects Havana with Pinar del 
Rio, lies the higher and drier portion of the Chirigota savanna. 
In its gravelly soil more or less mixed with grains of limonite, 
is growing a palm (Sabal sp.) closely related to the palmetto of 
the southeastern States, and, among lower plants, Sporobolus 
indicus is predominant in many places. In that environment, 


* The following specimens from other localities are in the herbarium of The 
New York Botanical Garden: pine-woods, Herradura (Earle 748); royal palm 
savanna, Herradura (Brillon, Earle & Gager 6342); coastal plain near Coloma 
(Britton & Gager 6006). The plant is also in the herbarium of Columbia Univer- 
sity, as found by Charles Wright (2046), presumably in Pinar del Rio, and this 


was the collection recorded by Grisebach as Sida ciliaris L.—F. W. PENNELL. 


the plant on which the new species is based attracted our atten- 
tion by its abundant and hirsute foliage and its relatively large 
yellow flowers, perhaps the most showy of all Cuban Sidas. 

The specimens collected had been at first tentatively referred 
to Sida ciliaris L., many characters being common to both 
species: Stems prostrate, hirsute-strigose, diffusely branching 
at base; leaves crenate or serrate above the middle; flowers clus- 
tered at the end of branches; long-ciliate linear or spatulate 
stipules. Remembering how the living plant differed in aspect 
from S. ciliaris | thought it likely to be a distinct species. 
In fact a more accurate observation revealed a number of dis- 
tinct characters. At first sight, the mode of branching and the 
distribution of leaves appear very different; in S. Brittoni the 
numerous stems which branch only near the base and have 
their nodes approximate, are leafy and nearly simple most of their 
length, while in S. czliaris the stems, shorter and thinner and 
with relatively long internodes brangh repeatedly throughout 
and most of the leaves are crowded near the extremites of the 
branches and around the inflorescence. 

Among other differences are the following: S. Brittoni has the 
leaves hirsute on both surfaces, the corolla yellow, the style- 
branches red and 4 mm. long, the top of the fruit puberulent 
and sharply reticulate-wrinkled; in S. ciliaris the leaves are 
glabrous on the upper surface and stellate-pubescent beneath, 
the smaller corolla reddish purple, the style-branches pale 
yellow, 2 mm. long, the top of the fruit tubercled and stellate- 
pubescent. 

As to the habitat it appears to be also different, Sida ciliaris 
being mostly confined to the sandy or rocky limestone soil of 

- coastal thickets and adjacent hillsides. 

This species is named in honor of Dr. Nathaniel Lord Britton, 
who has contributed so much to the knowledge of the Cuban 
flora. 


COLEGIO DE LA SALLE, 
VEDADO, HABANA. 


174 


A COMPARISON (OF THE PLORA OF SOUTHERN 
BRITISH, COLUMBIA WINE EA Ol seats 
SPATE SOR WASHINGLON. AS MEE US= 
TRATED BY THE PLORAS OF 
HENRY AND PIPER 


By JAMES C. NELSON 


The Pacific Northwest, by which rather elastic term may be 
understood the region extending from the northern boundary of 
California to Prince William Sound, Alaska, and including the 
present States of Oregon and Washington and the Province of 
British Columbia, has been a fruitful field for botanical research 
since the days of Archibald Menzies, and still affords ample 
opportunity for scientific investigation. Not only does it possess 
a vast and diversified fiora, with many species of restricted range 
and habitat, but there exists a marked tendency toward vari- 
ability, indicating that in’ this geologically recent portion of 
the continent, the process of evolution is still active also in the 
plant world, and affording strong support to the upholders of 
the ‘‘mutation”’ theory. As a result of this tendency to varia- 
tion, the limits of many species are not yet defined, and the 
relatively few students of the native flora have found themselves 
unable to cover the field adequately, so that anything like a 
comprehensive treatment of the flora of the entire region has 
not yet appeared. The rapid introduction of foreign species, 
which find in our genial climate and fertile soil conditions almost 
ideal for their speedy naturalization, still further complicates 
the situation. The Flora of Howell, that indefatigable pioneer, 
whose lack of scientific training was compensated for by a bound- 
less enthusiasm and a keen and accurate power of observation, 
has now become almost obsolete, so that the present-day student 
of the Northwest flora is compelled to have recourse to a com- 
paratively scanty list of local manuals, of very uneven scientific 
merit. It is a matter for congratulation therefore that Professor 
Henry has given to the scientific world in his recent manual* 


* Henry, Joseph Kaye. Flora of Southern British Columbia and Vancouver 
Island. Toronto: W. J. Gage & Co. Ltd. 1915. Pp. 363. $1.00. 


the result of his long and careful study of the Northwest flora. 
The book has been adopted for use by the schools of the Province, 
and in fact grew out of Professor Henry’s desire to provide for 
youthful students of the local flora a guide such as in his own 
youth he was unable to secure. The limitations of a school 
text have of course made it impossible for him to enter into 
technical taxonomic discussions, to give detailed statements 
of geographical range, or to confirm the included species by lists 
of specimens examined; but the descriptions are full and accurate, 
the keys carefully constructed, and a considerable number of 
new species and varieties are added to those already known to 
exist. 

The author displays a sound and sane conservatism, and has 
not looked with favor on the minuter classification of the North 
American Flora. The tendency toward excessive subdivision 
of genera and multiplication of species has gone very far in the 
last two decades, and must, to use Professcr Henry’s words, 
‘‘soon give place to the broader conception of what the ‘lumper’ 
considers constitutes a species.’’ We accordingly find that 
many recently proposed genera are restored to their original 
position. Piperia and Limnorchis are replaced in Habenaria, 
Batrachium in Ranunculus, Gormania in Sedum, Comarum, 
Dasiphora, Argentina and Drymocallis in Potentilla, Sieversia in 
Geum, Anogra and Onagra in Oenothera, Oxycoccus in Vaccinium, 
Harrimanella in Cassiope, Collomia in Gilia, Thalesia in Orobanche, 
Rapuntium in Lobelia, Eucephalus and Machaeranthera in Aster, 
and Ptilocalais in Microseris. Perhaps an excess of conservatism 
is shown in the return of Schizonotus to Spiraea and Navarretia 
to Gilia; but on the whole the tendency is toward a thoroughly 
sane conception of taxonomic relations. This is further illus- 
trated by the refusal to recognize the recent union of Papaver- 
aceae with Fumariaceae and Lobeliaceae with Campanulaceae, 
or the attempt to segregate Rosaceae into a group of too-closely 
related families. The nomenclature is throughout that of the 
International Rules, in strong contrast to the prevailing tendency 
among Western botanists to adopt the provincialities of the so- 
called ‘‘American’’ Code. While the Rules adopted at Vienna 


176 


are far from being adequate, they still represent the only method 
by which a satisfactory nomenclature can ever be attained, that 
of international agreement: and the attempt of any nation to 
herd by itself in these matters cannot hope for any greater success 


’ 


than the proposal of the ‘“‘free-silverites’’ in the matter of a 
monetary standard. 

Perhaps a more just estimate of the scope and value of Pro- 
fessor Henry’s work may be attained by comparing it with 
another manual covering an adjacent field. In 1906 Professor 
C. V. Piper published a Flora of Washington (Contr. U.S. Nat. 
Herb., Vol. XI), which still remains in many ways a model of 
scientific accuracy and thoroughness. Since Washington ad- 
joins British Columbia on the south, considerable resemblance 
between the floras of the two regions would be expected, and the 
majority of the species mentioned in the one manual might with 
reason be looked for in the other. 

A glance at the map, however, will show that this expectation 
of similarity must not be carried too far. Washington extends 
240 miles south of British Columbia; and no tendency in plant- 
distribution is more marked than the increase in the number of 
species away from the arctic regions and toward the tropics. 
The distinctively Californian flora which extends northward 
through Oregon and into Washington with a steadily diminish- 
ing number of representatives, seems to have reached its northern- 
most limit, in the case of the vast majority of species, in the 
neighborhood of a boundary which coincides more or less roughly 
with that of southern British Columbia. What may be termed 
the Alaskan or sub-arctic flora in like manner seems to have 
reached the limits within which it may be called dominant some- 
where north of the 49th parallel; and although many of its mem- 
bers continue southward in the Rockies, this region lies too far 
eastward of the eastern boundary of Washington to have much 
influence on the flora of that state. 

The exact limits of Henry’s manual are not very clearly de- 
fined to the northward. In his own words, ‘‘The region covered 
is mainly the southern part of the province extending from Van- 
couver Island to the Rockies, with a rather indefinite northern 


’ 


limit, to about the Skeena.”’ Since the valley of the Skeena, 
with its embouchure at Prince Rupert in latitude 54°, does not 
cross the entire breadth of the Province, but is replaced on the 
eastern slope by the valley of the Peace and its tributaries, it 
becomes somewhat difficult to fix an exact northern limit. But 
in any case the territory covered by this manual cannot be less 
than twice as large as the State of Washington, and extends far 
enough to the east to take in the entire western slope of the 
Rocky Mountain region, which lies far to the eastward of any 
part of the State of Washington, so that the casual observer 
would not unreasonably assume that of the two Floras, Henry’s 
would surpass Piper’s in the total number of species. But over 
against this hasty generalization must be set the fact, not only 
of the steady increase of species from the poles toward the 
equator, but the further consideration that the Upper Sonoran 
Zone, which dominates the semi-arid portion of eastern Washing- 
ton, and which is remarkably rich in number of species, is very 
scantily represented in the Province, extending but a short 
distance into the central plateau along the valley of the Okanogan. 
More than this, Washington is characterized by an endemism 
that is far less marked in the part of British Columbia under 
consideration. The number of species that have been reported 
from their type-locality only is surprisingly large; the Olympics, 
the Wenatchee Mountains, and Mount Rainier are all charac- 
terized by a strongly local flora; and the general region of the 
Columbia Gorge, including the greater part of the Columbia 
Valley from the Great Falls at Celilo to the sharp northward 
bend of the river at Pasco, contains a surprisingly large number of 
species with a very restricted local range. No such marked 
tendency to endemism seems to be displayed in any part of 
British Columbia. While the flora of Vancouver Island is 
perhaps the richest in species of local occurrence, and while 
there is a well-defined succession of botanical areas as we ad- 
vance eastward from the region of coast forest into the dry in- 
terior, and then through a second humid belt to the subalpine 
and alpine Rocky Mountain zones, the fact remains that the 
tendency to diversity is less marked in British Columbia than in 
Washington. 


178 


We must not be surprised therefore to find that while the 
total number of species, varieties and named forms included in 
Henry’s Flora is 2,359, the total enumerated by Piper reaches 
2,511. Of this number, allowing for differences in nomenclature 
and in the views held by the two authors regarding specific 
limits, and excluding 28 of Henry’s species that are definitely 
rejected by Piper, there are common to both manuals 1,517 
named forms: in other words, at least 60 per cent of all the species 
mentioned are common to both districts. 

In Henry’s Flora there are 764 species and forms not men- 
tioned by Piper; in Piper’s Flora 928 not mentioned by Henry. 
Doubtless if the present reviewer were thoroughly conversant 
with the taxonomic history and bibliography of all these forms, 
it would be possible to reduce these figures materially by detect- 
ing identity in names that seem wholly unrelated; but neither 
his knowledge nor the resources at his command permit such an 
undertaking. 

Retaining the above totals therefore, a few remarks may be 
offered on the species which appear in but one of the two manuals. 
In presenting these observations, the reviewer must presume that 
both authors have covered their territory with equal thorough- 
ness. In Professor Piper’s Flora, the author has appended to 
each species a full list of “‘Specimens Examined,” so that it is 
possible to confirm very definitely each and every one; but the 
scope of a school text-book has not permitted Professor Henry 
to do this, so that a full confirmation of his species cannot be 
attained. 

Assuming therefore that the 764 species mentioned only by 
Henry are all essentially different from any forms included by 
Piper, and that their existence within his territory can be defi- _ 
nitely confirmed, we find that they can be grouped approximately 
as follows: 

Two hundred and ninety-six belong to the Rocky Mountain 
flora, of which at least 40 may also be regarded as Alaskan, and 
21 occur also on Vancouver Island; 130 are distinctly Vancouver 
Island species, including the 21 found also in the Rockies and 12 
which are also Alaskan; 123 may be regarded as Alaskan, in- 


179 


cluding the 40 which occur also in the Rockies and the 12 also 
on Vancouver Island; 52 species, judging from the localities indi-” 
cated, are purely local (doubtless in many cases an unwarranted 
assumption); I1 are mentioned without definite locality or range; 
III are introduced species, of which 48 are personally known to 
the reviewer as occurring in Oregon, and therefore to be expected 
in the intervening territory of Washington: 50 are included and 
assigned to definite Washington stations in the two recent 
manuals by Piper and Beattie, the Flora of Southeastern Wash- 
ington and Adjacent Idaho (1914) and the Flora of the North- 
west Coast (1915). Several others of Henry’s species appear 
in the last-named work, but assigned only to Canadian stations. 

In addition to the above, there are 57 species which are given 
a range by Henry that either explicitly refers them to Washing- 
ton, or brings them so near the border that it would seem reason- 
able to expect them on the other side, but which find no mention 
in Piper’s Flora or the two later works of which he is joint author. 
This comparatively small margin of discrepancy would be 
doubtless further reduced by a wider knowledge of the specific 
and varietal limits of these forms, and a more thorough explora- 
tion of the territory. 

Turning now to the reverse side of the comparison, and ex- 
aming the 928 forms included by Piper but not mentioned by 
Henry, we find that they fall into several clearly-defined groups. 
Beginning with those of the most restricted range and. proceeding 
outward, we may roughly group them as follows: 

I. Species that have been reported from the type-locality 
‘only, 67. 

2. Species that belong to regions of marked endemism, with- 
out being restricted to the original station: 

In the Olympics, 15 

On Mount Rainier, 8 

In the Wenatchee Mountains, 21 
In the Columbia Gorge and 
Klickitat County, 96. 

3. Species occurring only in Washington, without restric- 
tion to one of the above regions, 107. 


180 


4. Species not occurring south of Washington, but with an 
eastern range, to Idaho, Montana, Colorado, etc., 72. 

5. Species occurring in Washington and Oregon only, 114. 

6. Species not occurring south of Oregon, but with an east- 
ward range, 67. 

7. Species extending from Washington to California, Nevada 
or Arizona, 364. 

Of the above list, 115 are species that are definitely referred ~ 
by the author to the Upper Sonoran Zone. 

The number of these Washington species which are either re- 
ferred outright to British Columbia in Piper’s statement of 
range, or given a range that would justify us in expecting them | 
in the Province, is 107, of which 19 are introduced. In both 
manuals therefore, the extreme margin of probable error is not 
excessive. 

A careful study of all these differences and discrepancies leads 
to two conclusions: 

1. That Washington, partly because of the different climatic 
conditions due to its more southern position, and partly because 
of its topography, is a region of more marked endemism than 
British Columbia. 

2. That although artificial boundaries are usually wholly 
without significance in determining plant-distribution, the 49th 
parallel seems to come very near to a line that marks the extreme 
northward dominance of the Californian flora on the one hand, 
and the extreme southern extension of the Alaskan or sub-arctic 
flora on the other. As far as the introduced plants are concerned, 
their occurrence or non-occurrence is a matter of very slight 
significance, since their establishment at any particular station 
is usually the result of pure accident, and no obstacle to their 
further spread will usually exist. Some further details of the 
differences between the two Floras may be of interest. 

Fifty-five genera represented in Henry are not found in Piper, 
but 30 of these include only introduced species (among these 
Ulmus with 3 species, Dianthus, Cynosurus and Vinca with 2 
each, and 26 others with one each). Androsace with 4 species is 
the largest indigenous genus not represented in Piper, next come 
Limnanthes and Primula with 2 each, and 22 others with one each. 


181] 


Piper’s Flora on the other hand includes 76 genera not men- 
tioned by Henry, of which only 3 (Syntherisma, Dipsacus and 
Cnicus) are introduced. The largest indigenous genus not 
represented in Henry is Sifanion with 11 species. Next to this is 
Capnorea with 5, Sphaerostigma and Frasera with 4, Hemicar- 
pha, Horkelia, Taraxia and Madronella with 3, and Parrya, 
Thermopsis, Elatine, Pachylophus, Trichostema and Tonella with 2; 
59 other genera are represented by a single species. 

The following table represents the discrepancies in the two 
Floras in the case of a few of the larger genera, particularly of 
those that reach their widest extension in the Northwest: 


Nm Piper’ | in Henry’ | Common | Piper Only | Henry Only 
SEUDVE. 5 e ee ae ie Bene 33 27 18 I5 9 
ChAT s 2 Bio Cee OO ee 108 | 40 61 52 65 
LORS BUR Ee 33 | 31 24 | 10 7 
SNES a Seas ang Ce eee 23 39 18 7 21 
EO POMUNI Cribs ss. 653 6 ss 28 10 6 23 4 
GUUS ONUIE po, ec ive rch Bas 22 sy 34 30 24 I2 6 
RILIRETECILLILS ici e355 2-5 3500 2 30 34 21 9 13 
wa IT Tcl AACS ke a 20 12 Io sa6) 2 
DTA PRILOIE e ie. oss dees ei sveu0!s 18 32 I2 7 20 
COLOIIULE Ee rents feces 29 28 18 8 10 
LPT ES Aes Ce RCE Oe RTE 35 22 | 15 20 ii 
JAS TUTTE a eae 38 THe) th 13 20 6 
WOME rte 2s Sc upete coe sh oeye 20 23 I5 6 8 
ILA TITLE a BR OR CnC 23 II 9 15 2 
TOE SLEMOIE PN Nstl ess Sis wt ee 27 I2 Io 7 2 
GG? 2 RR CRE ee Cree 32 27 16 16 Eg 
LEG AAG AQ) Jee OR CEEE ME ARCTIC 25 37 18 8 | 19 
SHHOUTD Sepiee SOOO eon eae: 31 32 17 I4 15 


These figures seem to show that in genera with a predominantly 
northern range, Henry’s total of local species will exceed Piper’s; 
while in those with a southern range the converse will be true. 
In the case of Carex, about all that seems to be illustrated is 
the fact that neither author had been able to make an exhaus- 
tive study of the genus or arrive at any clear understanding of 
its species. It is to be hoped that the much-needed clearing- 
up of this difficult problem will be attained by the careful work 
which K. K. Mackenzie is now doing on the genus. In matters 
of form and technique, which with a few notable exceptions 
remain the weak point of American authors, the reviewer re- 


182 


grets to note considerable carelessness in Professor Henry’s 
book. He announces in his preface his intention of capitalizing 
only ‘‘some old Linnean generic names still retained for species 
and those derived from the names of persons’’; but on the one 
hand we find him writing Italica, Monspeliensis, Major, Sibiri- 
cum, Beeringianum, Andina, Davuricum, Moschatus, and on 
the other convolvulus, paronychia, cymbalaria, aquifolium, malus, 
parthenium as specific names. 

Occasionally he overlooks the fact that under the International 
Rules trinomials are not written without an indication of the 
category of the third member, as subspecies, variety or forma, 
and we read Populus nigra Italica, Anemone patens Wolfgangiana. 
In general, however, the subdivisions of species are more clearly 
differentiated than in Piper, whose disposition to regard the 
43 as identical has led to much 
confusion. But Henry does not always avoid the absurdity of 
identical binomials, as Phegopteris phegopteris, Hypopitys 
hypopitys (misspelled in the text). Failures in grammatical 
agreement are far too common, such as: Equisetum arvensis, 


7 ? 


terms “‘subspecies”’ and “ variety’ 


Equisetum variegatum var. Alaskana, Pleuropogon refractum (an 
error to which most Western writers stubbornly cling), Cypri- 
pedium parviflora, Gormania oreganum, Sedum rosea, Rubus 
viburnifoa, Geum humilis, Acer circinatum var. fulva, Malva 
moschatus, Phyllodoce glanduliflorus, Mimulus Lewisi var. alba, 
Mimulus Langsdorfi var. minima, Symphoricarpos racemosa, 
Aster Lindleyana, Erigeron membranaceum, A goseris villosum. 

This carelessness is the more regrettable, since several of these 
blunders are found in the case of new species and varieties pro- 
posed by the author! 

Orthographical blunders are so common as to make us wonder 
whether the author read his proof at all. In the case of generic 
names we are compelled to read: Hordum, Commandra, Hesperus, 
Hypopites, Asperuga, Eriganum, Seriocarpus: and in specific 
names: Poa Fenderiana, Papaver sominferum, Alyssum alysoides, 
Cakile edulenta, Philadelphus Lewesit, Boykinia circinnata, 
Potentilla monspielensis, Cymopterus terebinthus, Boschniakia 
strobiliacea, Campanula rotundifolia var. petiotala, Xanthium 


183 


candense and Coreopsis Atkinsonia. The name of the Water- 
Lily Family is spelled Nymphaceae. ‘Trelease’s name appears _ 
as “ Trealease,’’ Betcke’s as ‘“‘ Betche,’’ and Moquin is abbrevi- 
ated ‘‘ Mog.” 

In this matter of abbreviations the author seems to have pro- 

ceeded on the theory that variety is the spice of life, and along 
with the accepted forms he occasionally treats us to the following: 
Haus. for Haussknecht, Bick. for Bicknell, Wat. for Watson, Par. 
for Parlatore, Mich. for Michaux (wholly forgetting that this 
abbreviation belongs to Micheli), Scrib. for Scribner, Mer. for, 
Merrill, Thur. for Thurber, Vil. for Villars, Buck. for Buckley, 
Hitch. and Hitche. for Hitchcock, Brit. for Britton, Beuth. for 
Bentham, Fer. for Fernald, Englem. for Engelmann, Ren. for 
Rendle, Walle. and Walls. for Wallroth. 
Often the abbreviation is written without the period, as if it 
were the full name, as Rosen, Lindl, Schrad, Bickn, Led, Hook, 
Kaulf, Lamb, ... On the other hand, full names are fre- 
quently written as if abbreviations (Hoppe., Presl., Morong.). 
Presl also appears as Pris] and Wiegand as Weigand. 

The authority for species is often omitted entirely, as in the 
case of 

Polygonum Nuttallit, which should be assigned to Small 


Polygonum minimum “ of if Watson 
Myosurus minimus a * a Linnaeus 
Onobrychis sativa i ri s Lamarck 
Papaver somniferum # ‘s Linnaeus 
Medicago arabica 7 ‘ ss Hudson 
Erigeron filifolius ¥ a _ (Hooker) 
Nuttall 


Citations of authorities are frequently incorrect. 

Puccinellia angustata (R. Br.) R. & R. should be (R. Br.) 
Nash. 

Lysichiton kamtschatcense Schott should be (L.) Schott. 

Corylus californica Rose should be (A.DC.) Rose. 

Sagina occidentalis Green [sic] should be Wats. 

Vancouveria hexandra M. &. C. should be (Hook.) Morr. & 
Dec. 


184 


Athysanus pusillus Greene should be (Hook.) Greene. 
Cytisus scoparius Link should be (L.) Link. 

Circaea pacifica Arch. [sic] should be Aschers. & Magn. 
Valerianella samolifolia Haeck. should be (DC.) A. Gray. 
Chrysopsis villosa Nutt. should be (Pursh) Nutt. 

Such miscellaneous inaccuracies as ‘‘Fallarone Is.’’ for Faral- 
lone: “L. Her.”’ for L’Her. and ‘‘D. C.” for DC. are also encoun- 
tered. The species Montia parviflora appears twice, and M. 
parvifolia as a consequence wholly disappears. After Epipactis, 
“R.BR.” is written where the common name is usually given. 
Elsewhere authors of genera have not been cited. 

A praiseworthy attempt has been made to indicate the deriva- 
tion of generic names; but 141 genera are left unexplained, and 
in the case of others such absurd blunders as Peramium from 
“per, through, amium, love, in allusion to medicinal properties”’ 
(no such word as “‘amium”’ exists in the Latin language), Hu- 
mulus, “dim. of humus, the ground, because sometimes pros- 
trate”’ (the root is Teutonic, and has no relation to the Latin 
humus) and Malvastrum from “‘ Malva and aster, a star’? (when 
it is simply the contemptuous diminutive) are perpetuated, 
evidently all borrowed from Frye and Rigg’s Northwest Flora, 
which as a masterpiece of etymological inaccuracy can hardly 
be surpassed. Nuttall and Pursh are hardly to be regarded as 
“English” botanists, when their period of greatest scientific 
activity was spent in the United States. 

In spite of these regrettable defects of form, however, the 
impression left by Professor Henry’s book is, that it is a praise- 
worthy and valuable effort to contribute to the fuller knowledge 
of the Northwest flora, and that the work has been surprisingly 
well done considering that the author makes no claims to being 
a professional botanist. It is only by such local studies that a 
full understanding of the fascinating but difficult flora of the 
Northwest can ever be reached; and it is to be hoped that at 
some future time Professor Henry may shake off the limitations 
imposed by a school text, and revise his manual in strictly sci- 
entific form. 


SALEM, OREGON 


185 


NEWS ITEMS 


Mr. A. O. Garrett, head of the department of Botany, Salt 
Lake High School, had an appointment and worked as Field 
Assistant in the Blister Rust Control during the past summer. 


During the early part of the year Mr. Joseph F. Rock’s 
Monographic Study of the Hawaiian Lobelioideae, a splendidly 
illustrated quarto volume, was issued by the Bernice Pauahi 
Bishop Museum, Honolulu. 


The United States National Museum has just issued as volume 
21 of its Contributions a Flora of the District of Columbia by A. 
S. Hitchcock and Paul C. Standley. The authors had the assist- 
ance of the botanists of Washington in the undertaking. Over 
1600 species and 649 genera are noted in the book, which treats 
of the species growing in the District and their distribution. 


Mr. Camillo Schneider, after spending several years in this 
country and naming the willow collections in most of the larger 
herbaria of the country, sailed for Vienna on September 3. 


Dr. Carl Skottsberg has assumed the directorship of the new 
botanical garden at Géteborg, Sweden. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of TorRREYA in which their papers appear, will kindly notify the 
editor when returning proof. 4 

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New Era Printing Co., 41 North Queen Street, Lancaster, Pa., have furnished the 
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Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs. E. G. BRITTON, Chairman. 
J. H. BARNHART, Pror. JEAN BROADHURST 
Miss C. C. HAYNES B. O. DoDGE 
SERENO STETSON MICHAEL LEVINE 
. Budget Committee F, J. SEAVER 
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R.A. HARPER J. K. SMALt, Chairman. 
N. L. Britton T. E. HAZEN 
A. W. Evans E. W. OLIVE 
M. A. Howe Local Flora Committee 
H. H. Russy : N. L. Britton, Chairman. 
Field Committee Phanerogams: Cryptogams: 
F. W. PENNELL, Chairman. E. P. BICKNELL Mrs. E.G. BRITTCN 
Mrs. L. M. KEELER N. L. BRITTON T. E. HAZEN 
MICHAEL LEVINE Ty 4G. 6. Curtig M. A. Howe 
GEORGE T. HASTINGS : K. K. MACKENZIE MICHAEL LEVINE 
PERCY WILSON NORMAN TAYLor, W.A. MuRRILL 


F. J. SEAVER 
Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M. Richards, F. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurs 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


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CONTENTS 
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Roosevelt’s Notes on Brazilian Trees... -........ccccssccccs seecccecsecctnecsseesecescs Ceseeeuee 194 
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TORREYA 


Vol. I9 No. 9 
October, IgI9 


NOTES ON THE GRASSES OF HOWELL’S FLORA OF 
NORTHWEST AMERICA 


By JAMES C. NELSON 


Every student who makes a serious attempt to become familiar 
with the flora of Washington or Oregon, must acknowledge his 
obligation to the great work of Thomas Howell. The adjective 
is used advisedly. When we take into account the author’s 
lack of scientific training, the very limited herbarium and library 
resources at his command, the scarcity of congenial associates, 
and the constant financial burdens under which he labored, and 
then observe the total of species and forms which he was able to 
recognize, the number of new species which he published, the 
keenness of his observation and the soundness of his critical 
judgment, we can hardly avoid the conclusion that’ here was a 
scientist who with better preparation and under a more favor- 
able environment would have been worthy of rank with John 
Torrey or Asa Gray. With all its inevitable defects, his Flora 
must remain a land-mark in the history of Western botany, and 
the essential soundness of his fundamental conclusions is being 
vindicated daily. Nor do we detract in any way from the value 
of his work, or cast any aspersion on his scientific conscience, 
when we venture to point out that the Flora has from the be- 
ginning been in need of revision, and has in many respects be- 
come almost obsolete since its publication in 1893. Howell 
himself, had he lived, would have taken full account of the 
advances in botanical knowledge, and would have been the 
first to suggest a revision of his Flora. 

In the course of an attempt to become familiar with the grasses 
of Oregon, particularly of that part of the state included in the 


[No. 9, Vol. 19 of TORREYA, comprising pp. 161-185, was issued October 28, 1919.] 


187 


188 


Willamette Valley, the present writer has found it necessary to 
make the following notes on the Gramineae (pp. 713-781) in 
his interleaved copy of Howell’s Flora: 


I. SpEctEs Not INCLUDED WHICH HAVE SINCE BEEN FOUND IN 


VARIOUS LOCALITIES IN OREGON 


1. Paspalum dilatatum Poir. On ballast at Linnton. 


. Panicum barbinode Trin. With the last. 


3. Panicum pacificum Hitche. & Chase. On gravelly prairies 


co N 


and along streams throughout the Willamette Valley. 


. Panicum thermale Boland. On rocky shore of Rogue River 


near Agness, Curry County. 


. Panicum miliaceum L. On rubbish-heaps about Salem. 
. Digitaria humifusa Pers. On sand-bars in the Willamette 


River, and beginning to appear on lawns in Salem. 


. Phalaris minor Retz. On ballast at Linnton. 
. Phalaris paradoxa L. var. praemorsa Coss. & Dur. With 


the last. 


. Phalaris brachystachys Link. With the last. 

. Cenchrus carolinianus Walt. With the last. 

. Setaria wmberbis Poir. With the last. 

. Anthoxanthum Pueli Lecog & Lamotte. Not uncommon in 


dry, especially alkaline, soil throughout the Willamette 
Valley. 


. Agrostis pallens Trin. On sand-dunes along the coast. 
. Agrostis alba L. var. maritima (Lam.) Mey. Common on 


' sand-dunes and in salt-marshes along the coast. 


. Cynodon Dactylon L. On ballast at Linnton, and beginning 


to appear in cultivated ground about Eugene. 


. Ammophila arenaria (L.) Link. On ballast at Linnton. 

. Apera spica-venti (L.) Beauv. Ona lawn at Salem. 

. Nassella chilensis Desy. On ballast at Linnton. 

. Eleusine tristachya Kunth. With the last. 

. Chloris radtata Sw. With the last. 

. Stipa littoralis Phil. With the last. 

. Stipa Lemmoni Scribn. var. Jonesii Scribn. On dry slopes 


in southwestern Oregon. 


23. 
24. 


25. 
26. 
2>. 


28. 
29. 


30. 
an. 
32: 


33: 


34- 
35: 
36. 
37: 
38. 
39. 
40. 
4I. 


42. 
43. 


189 


Lepturus incurvatus Trin. On ballast, Linnton. 

Aira capillaris Host. On sand-bars along the Santiam 
River, and in cultivated ground at Salem. 

Deschampsia holciformis (Presl) Steud. On dry soil at 
summit of ocean bluffs on Yaquina Head. 

Avena barbata Brot. Becoming common along the rail- 
road near Salem. 

Eragrostis cyperoides (Thunb.) Beauv. On ballast at 
Linnton. 

Eragrostis Orcuttiana Vasey. With the last. 

Panicularia occidentalis Piper. Common in ditches in 
the region about Salem. 

Cynosurus cristatus L. Occasional on lawns at Salem and 
Eugene. C. echinatus L. is reported by Mr. V. R. Brad- 
shaw as spreading rapidly in the vicinity of Eugene. 

Poa trivialis L. Not uncommon in shady places throughout. 

Poa alcea Piper. In rocky woods at Elk Rock, Multno- 
mah County. 

Puccinellia paupercula (Holm) Fern. & Weath. var. alaskana 
(Scribn. & Merr.) Fern. & Weath. Not infrequent in 
salt-marshes and on sea-beaches along the coast. 

Festuca megalura Nutt. Abundant in dry soil almost 
everywhere. 

Festuca bromoides L. Common in cultivated ground and 
along railroads. 

Festuca rubra L. var. megastachys Gaudin’ Occasional on 
roadsides. 

Scleropoa rigida Griseb. Around old eines in the 
business district of Salem. 

Lolium multiflorum Lam. Abundant in waste and culti- 
vated ground everywhere. 

Lolium perenne L. var. cristatum Doell. <A single specimen 
in a wooded ravine near Eola, Polk County. 3 

Agropyron caesium Presl. Dry soil about light-house on 
Yaquina Head. 

Agropyron junceum Beauv. On ballast at Linnton. 

Agropyron glaucum R. &.S. With the last. 

Agropyron pungens (Pers.) R. & S. With the last. 


190 


Il. SpEciES WHOSE EXISTENCE IN THE TERRITORY DoOEs Not 


lis 


SEEM TO BE CONFIRMED 


Panicum capillare L. Although some of the Oregon forms 
seem to approach this species, it seems best to refer them 
to P. barbipulvinatum Nash. 


2. Panicum pubescens Lam. 
3. Panicum dichotomum L. Both of these seem referable to 


P. occidentale Scribn. 


. Panicum scoparium Lam. Evidently P. Scribnerianum 


Nash. 


. Aristida fasciculata Torr. Probably A. bromoides HBK., 


and its occurrence very doubtful. 


. Melica interrupta Trin. The name seems to be incorrectly 


applied. 


. Panicularia fluitans Kuntze. Probably P. leptostachya 


(Buckl.) Piper. 


. Poa glauca Vahl. An introduced species—not confirmed 


by any later collector. 


. Festuca heterophylla Lam. Probably F. occidentalis Hook. 
. Elymus dasystachys Trin. Apparently not correctly applied. 


. SPECIES WHOSE TAXONOMIC LIMITS ARE NOW GENERALLY 


UNDERSTOOD DIFFERENTLY 


. Panicum sanguinale L. = Digitaria sanguinalis (L.) Scop. 

. Panicum crus-galli L. = Echinochloa crus-galli (L.) Beauv. 
. Phalaris amethystina Trin. = P. californica Hook. & Arn. 
. Sporobolus cuspidatus Wood = S. Richardsonit (Trin.) 


Merr. 


. Sporobolus depauperatus Scribn. = Muhlenbergia squarrosa 


Rydb. 


6. Sporobolus Bolanderi Vasey = Poa multnomae Piper. 


. Sporobolus gracillimus Vasey = Muhlenbergia filiformis 


Rydb. 


8. Sporobolus simplex Scribn. = Muhlenbergia filiformis Rydb. 
9. Sporobolus filiformis Scribn. = Muhlenbergia filiformis 


10. 


Rydb. 
Agrostis asperifolia Trin. = A. exarata Trin. 


191 


. Agrostis grandis Trin. = A. exarata Trin. 

. Agrostis Scoulert Trin. = A. exarata Trin. 

. Agrostis densiflora Vasey = A. glomerata (Presl) Kunth. 

. Agrostis verticillata Vill. = A. stolonifera L. 

. Agrostis tenuiculmis Nash = A. idahoensis Nash. 

. Agrostis Pringlet Scribn. = A. Halli Vasey var. Pringlei 


(Scribn.) Hitchce. 


. Agrostis geminata Trin. = A. hyemalis (Walt.) BSP. var. 


geminata (Trin.) Hitchce. 


. Agrostis attenuata Vasey. = A. oregonensis Vasey. 

. Agrostis scabra Willd. = A. hyemalis (Walt.) BSP. 

. Agrostis varians Trin. = A. Rossae Vasey. 

. Agrostis virescens HBK. Probably = A. ampla Hitchce. 

. Gastridium australe Beauv. = G. lendigerum (L.) Gaudin. 
. Cinna pendula Trin. = C. latifolia (Trev.) Griseb. 

. Calamagrostis lactea Beal = C. Langsdorfiit Trin. var. 


lactea (Beal) Kearn. 


. Spartina cynosuroides Willd. = S. Michauxiana Hitchc. 
. Stipa Kingit Boland. = Oryzopsis Kingit (Boland.) Beal. 
. Stipa Bloomert Boland. = Oryzopsis Bloomeri (Boland.) 


Ricker. 
. Stipa oregonensts Scribn. = 5S. occidentalis Scribn. 
. Stipa viridua Trin. = S. minor Scribn. 


. Oryzopsis cuspidata Vasey = O. hymenoides (R. & S.) 


Ricker. 


. Alopecurus geniculatus.L. var. robustus Vasey = A. gent- 


culatus L. 


. Alopecurus pallescens Piper = A. californicus Vasey. 
. Avena fatua L. var. glabrescens Coss. = var. glabrata 


Peterm. 


. Avena Smith Porter = Melica Smithii (Porter) Vasey. 


35: 
36. 


37: 


Trisetum barbatum Steud. = Bromus Trini Desv. 

Trisetum subspicatum Beauv. = T. spicatum (L.) Richter. 

Deschampsia calycina Presl = D. danthonioides (Trin.) 
Munro. 


* Farwell has recently established the genus Bromelica for this section of 
Melica (Rhodora 21: 76-78). 


38 


39- 


40. 


62. 


63. 
64. 


192 


Holcus lanatus L. = Notholcus lanatus (L.) Nash. 

Eatonia obtusata Gray = Sphenopholis obtusata (Michx.) - 
Scribn. 

Eatonia pennsylvanica Gray = Sphenopholis pallens 
(Spreng.) Scribn. 

Melica bulbosa Geyer = M. bella Piper. 

Melica bromoides Gray and var. Howellii Scribn. = M. 
Geyert Munro. 

Melica Harfordi Boland.. var. minor Vasey = subsp. 
tenutor Piper. 

Melica acuminata Boland. = M. subulata (Griseb.) Scribn. 


. Melica scabrata Scribn. = M. spectabilis Scribn. 

. Distichlis maritima Raf. = D. spicata (L.) Greene. 

. Panicularia nervata Kuntze = Glyceria elata Hitchc. 

. Poa reflexa Vasey & Scribn. = P. leptocoma Trin. 

. Poa tncurva Scribn. & Williams = P. Sandbergii Vasey. 

. Poa occidentalis Vasey & Scribn. = P. nervosa (Hook.) Vasey. 
. Poa purpurascens Vasey = P. paddensis Williams. 

. Poa flava L. = P. triflora Gilib. 

. Poa wnvazinata Scribn. & Williams = P. gracillima Vasey. 
. Poa Buckleyana Nash and var. stenophylla Vasey = P. 


scabrella Benth. 


. Eragrostis reptans Nees = E. hypnoides (Lam.) BSP. 
. Festuca microstachys Nutt. var. ciliata Gray = F. Grayt 


(Abrams) Piper. 


. Festuca microstachys Nutt. var. pauciflora Scribn. & Vasey = 


F. reflexa Buckl. 


. Festuca denticulata Beal = F. subuliflora Scribn. 

. Festuca californica Vasey = F. aristulata (Torr.) Shear. 
. Festuca Jonesit Vasey = F. subulata Trin. 

. Festuca brevifolia R. Br. = F. ovina L. var. brachyphylla © 


(Schultes) Piper. 
Festuca ovina L. var. polyphylla Vasey = F. occidentalis 
Hook. . 
Festuca ovina L. var. ingrata Hack. = F. idahoensis Elmer. 
a “«  « —« “columbiana Beal = F. idahoensis 
Elmer. 


* See note on no. 34 above. 


65. 
66. 
76. 


68. 
69. 


70. 
aT. 
rep 


7: 
74. 
75: 


76. 
77: 


78. 
79: 
80. 
81. 
82. 
83. 
84. 


85. 


193 


Festuca ovina L. var. oregana Hack. = F. idahoensis Elmer. 
Festuca scabrella Torr. = F. altaica Trin. 
Festuca rubra L. var. pubescens Vasey = var. Kitaibeliana 


(Schultes) Piper. 

Festuca rubra L. var. littoralis Vasey = var. pruinosa Hack. 

Bromus racemosus L. var. commutatus Hook. = B. com- 
mutatus Schrad. 

Bromus hordeaceus L. var. glabrescens Shear = var. lep- 
tostachys Beck. . 

Bromus Gussoni Parl. = B. villosus Forsk. and prob. var. 
Gussonei Aschers. & Graebn. 

Agropyron divergens Nees = A. spicatum (Pursh) Scribn. 
& Sm. 

Agropyron brevifolium Scribn. = A. violaceum Vasey. 

Agropyron Elmeri Scribn. = A. lanceolatum Scribn. & Sm. 

Agropyron dasystachyum [(Hook.) Scribn.] var. subvillosum 
Scribn. & Sm. = A. subvillosum (Hook.) Piper. 

Hordeum maritimum With. = H. geniculatum All. 

Elymus saxicolus Scribn. & Sm. = Agropyron flexuosum 
(Piper) Piper. 

Elymus mollis Trin. = E. arenarius L. 

Elymus littoralis Turcz. = E. arenicola Scribn. & Sm. 

Sitanion elymoides Raf. Prob. = S. Hystrix (Nutt.) Sm. 

Sitanion glaber J. G. Smith = S. rigidum Sm. 


Sitanton villosum J. G. Smith = S. jubatum Sm. 


Sitanion Leckenbyt Piper = S. planifolium Sm. 

Sitanion flexuosum Piper = Agropyron flexuosum (Piper) 
Piper. 

Sitanion Brodiet Piper = Elymus canadensis L. 


- To assert that all the above changes are accepted as universally 

valid is simply to assume the existence of a nomenclatorial tribu- 
nal whose decisions are everywhere accepted as final. Since a 
species is not an objective entity but a subjective concept, its 
limitations must in the end remain a matter of private judgment. 
Doubtless some modern agrostologists would retain many of 
Howell’s names: but it is believed that the changes suggested 
above approximate the present consensus of opinion regarding 
specific limitations. 


194 


ROOSEVELT'S NOTES ON BRAZILIAN TRESS 


Theodore Roosevelt was admittedly the world’s authority 
on the big game mammals of North America—and he was always 
greatly interested in birds—but his interest in trees and plants 
was not so keen. His observation of the fauna, however, did not 
prevent him from giving a thought to trees, particularly when 
they were striking or unusual. His book, “Through the Brazilian 
Wilderness”’ is full of interesting references to trees. 

It was always the dramatic that appealed to Theodore Roose- 
velt. He was interested in animals because they were full 
of action. Like Roosevelt himself, they did things. Even in 
his descriptions of trees it is interesting to note that it was their 
dramatic element and ‘not still charm that usually attracted his 
attention. For instances, here is a graphic description of 
parasitic fig-trees engaged in strangling a group of palms. Itisa 
picture of still life, yet it is dramatic: 

“Tn one grove the fig-trees were killing the palms, just as in Africa they kill the 
sandalwood trees. In the gloom of this grove there were no flowers, no bushes; the 
air was heavy; the ground was brown with moldering leaves. Almost every palm 
was serving as a prop for a fig-tree. The fig-trees were in every stage of growth. 
The youngest ones merely ran up the palms as vines. In the next state the vine 
had thickened and was sending out shoots, wrapping the palm stem in a deadly 
hold. 

“Some of the shoots were thrown round the stem like the tentacles of an immense 
cuttlefish. Others looked like claws, that were hooked into every crevice, and 
round every projection. In the stage beyond this the palm had been killed, and 
its dead carcass appeared between the big, winding vine trunks; and later the palm 
had disappeared and the vines had united in a great fig-tree. Water stood in 
black pools at the foot of the murdered trees, and of the trees that had murdered 


them. There was something sinister and evil in the dark stillness of the grove; it 
seemed as if sentient beings had writhed themselves round and were strangling 


’ 


other sentient beings.’ 
Later on he gives a more cheerful picture of tropic vegetation. 


““We passed through wonderfully beautiful woods of tall palms, the ouaouaca 
palm—wawasa palm, as it should be spelled in English. The trunks rose tall and 


* It is a pleasure to print this as a contribution to the movement to memorialize 
our greatest recent American, whose untimely death removed a much needed man 
of the hour. The Roosevelt Memorial Association of 1 Madison Avenue, New York, 
has kindly allowed, through the courtesy of Mr. Roosevelt’s publishers, the re- 
printing of these notes on trees collected during the now famous Brazilian Ex- 
pedition.—Eb. 


195 


strong and slender, and the fronds were branches twenty or thirty feet long, with 
the many long, narrow green blades starting from the midrib at right angles-in 
pairs. Round the ponds stood stately burity palms, rising like huge columns with 
great branches that looked like fans, as the long, stiff blades radiated from the 
end of the midrib. One tree was gorgeous with the brilliant hues of a flock of 
party-colored macaws. Green parrots flew shrieking overhead.”’ 


In this same book of Brazilian exploration, Colonel Roosevelt 
gives a fascinating picture of a journey up a stream picturesquely 
described as the “River of Tapirs.’’ He and his party went 
up this river in a launch, and the Colonel’s description of the 
scene reminds one of Joseph Conrad’s ‘‘ Heart of Darkness.”’ 

*‘Ahead of us,’ wrote the Colonel, ‘“‘the brown water stream stretched in curves 
between endless walls of dense tropical forest. It was like passing through a gigan- 
tic greenhouse. Wawasa and burity palms, cecropias, huge figs, feathery bamboos, 
strange foliage as delicate as lace, trees with buttressed trunks, trees with boles 
rising smooth and straight to lofty heights, all woven together by a tangle of 
vines, crowded down to the edge of the river. Their drooping branches hung 
down to the water, forming a screen through which it was impossible to see the 
bank. Rarely one of them showed flowers—large white blossoms, or small red or 
yellow blossoms. More often the lilac flowers of the begonia-vine made large 
patches of color. Innumerable epiphytes covered the limbs, and even grew on 
the roughened trunks.” 

There are frequent references to the wawasa palms and the 
Colonel noticed on one of them, a veritable giant in height, a 
mass of purple orchids growing from the side of the trunk, 
half-way to the top. On another big tree, not a palm, he saw 
more than a hundred troupials’ nests (the troupial is the South 
American oriole). He also mentions seeing palms of different 
varieties with short fronds. Wild plantains were plentiful and 
there were huge trees like those that grow in California. 

At other times the trees would be few and far between, or 
.else they would be scrubby and unprepossessing. 

“Day after day; we rode forward across endless flats of grass and of low open 
scrubby forest, the trees standing far apart and in most places being but little 
higher than the head of ahorseman. Some of them carried blossoms, white, orange, 
yellow, pink; and there were many flowers, the most beautiful being the morning 
glolies. Among the trees were bastard rubber trees, and dwarf palmetto; if the 
latter grew more than a few feet high their tops were torn and dishevelled by 
the wind.” 

Members of the Roosevelt party also found many fossil-tree 
trunks which the Colonel believed to be of Cretaceous age. 


196 


Here is a pretty picture that the Colonel paints: 


“In the deep valleys were magnificent woods, in which giant rubber-trees towered, 
while the huge leaves of the low-growing pacova or wild banana, were conspicuous 
in the undergrowth. Great azure butterflies flitted through the open, sunny 

~glades, and the bell-birds sitting motionless, uttered their ringing calls from the 
dark stillness of the columned groves.”’ 

While going down the famous River of Doubt, now the Rio 
Teodoro (River Theodore), the undergrowth was so dense that 
trees leaned over the river from both banks, forming barriers, 
which the men in the leading canoes cleared away with their 
axes. There were many palms and the Colonel noticed a hand- 
some species of bacaba. He also gives an interesting descrip- 
tion of stopping at a bee-tree to get honey. 

““The tree was a towering giant of the kind calléd milk-tree, because a thick 
milky juice runs freely from any cut,’’ he wrote. ‘‘Our camaradas eagerly drank 
the white fluid that flowed from the wounds made by their axes. I tried it. The 
taste was not unpleasant, but it left a sticky feeling in the mouth.” 

He also speaks particularly about the cajazeira tree, whose 
fruit he found delicious, and makes the suggestion that this fruit 
would make a valuable addition to our orchards, pointing out 
that, although tropical, the tree thrives when domesticated and 
propagates rapidly from shoots. He advises the Department of 
Agriculture to experiment and see if this tree would not grow in 
Southern California and Florida. 

While going down the Rio Teodoro, Colonel Roosevelt saw 
many trees, the tops of which were covered with yellow-white 
blossoms and red blossoms. Then he mentions a peculiarity 
that demonstrates his closeness of observation: 

“Many of the big trees were buttressed at the base with great thin walls of wood. 
Others, including both palms and ordinary trees, showed an even stranger peculi- 
arity. The trunk, near the base, but sometimes six or eight feet from the ground, 


was split into a dozen or twenty branches or small trunks which sloped outward in 
tent-like shape, each becoming a root. The larger trees of this type looked as if 


’ 


their trunks were seated on the tops of the pole frames of Indian tepees.’ 


While it was the fauna more than the flora that interested 
Colonel Roosevelt, as has been remarked at the beginning of this 
article, nevertheless his remarkable powers of observation were 
always in evidence, which lends interest to everything that he 


197 


describes, whether it is a lion charging upon him with the speed 
of an express train, trees that strangled each other, or trees that- 
dripped with honey when wounded. This observation was 
instinctive with Theodore Roosevelt because he was a born 
naturalist. 


SHORTER NOTES 


HELIANTHUS BESSEYI BATES. — Helianthus besseyi J. M. 
Bates was described in American Botanist, February, 1914, p. 17, 
from specimens collected at Red Cloud, Nebraska. Last spring 
Mr. Bates was kind enough to send me some of the tubers, which 
I planted in my garden at Boulder, May 5. The tubers are 
elongate-fusiform, and yellowish. Today (September 14) the 
plants are past flowering, though the closely related H. alexandri,* 
a few feet away, is in full bloom. The plants are about 5 feet 
high when well grown, and are strict, with comparatively few 
floriferous branches, entirely in the style of alexandri. The 
stems are reddish and scabrous, as in alexandri, but rougher. 
Leaves opposite, alternate above, as in alexandri. Leaves 
subovate, conspicuously broader than in alexandri, and some- 
what paler, the bases broad-cuneate, the petioles fairly long and 
distinctly winged. As in alexandri, the upper surface is rough, 
the lower soft-hairy, with the hairs on the midrib appressed. 
The rays are orange, as in alexandri, but are much shorter, 
about 30 mm. (in alexandri 41 mm. long and 14.5 wide). The 
achenes are the same in both, but the disc-corollas of besseyi are 
shorter, with paler lobes. The involucral bracts are spreading, 
but short (about 9 mm. long, base of involucre to end of longest 
phyllary about 12 mm.), with blackish bases (entirely pale green 
in alexandri), and there is the appearance of an extra row. The 
leaves are entirely dull above. The plant is quite distinct from 
H. nebrascensis (Ckll.), which also occurs at Red Cloud, and 
although it is close to the Michigan H. alexandri, it must evi- 
dently be separated from it, having a number of salient charac- 
ters. It adds one more to the assemblage of closely related 
species grouping around H. tuberosus. 


* Helianthus tuberosus alexandri Ckll., Amer. Naturalist, LIII: 188; H. alex- 
and1i Ckll., Monthly Bull. Calif. State Comm. Hoiticulture, VIII: 249. (1919.) 


198 


A matter for investigation is the relationship between H. besseyi 
and H. apricus Lunell, Amer. Midl. Nat, 1910, 237. The latter 
species, found on the open prairie in North Dakota, differs from 
besseyi by the narrower leaves, and the involucral bracts in two. 
rows. The description is not sufficiently detailed to permit 
adequate comparisons. In the herbarium of the New York 
Botanical Garden I have examined H. apricus camporum (Lunell), 
from the type lot. This variety has leaves shaped as in besseyz, 
but more remotely dentate, and (according to the description) 
scabrous beneath. H. nitidus Lunell, from the description, 
seems more like H. nebrascensis, but the rays are less than half 
as long.—T. D. A. COCKERELL 


BOULDER, COLORADO 


THE SUPPOSED SOUTHERN LIMIT OF THE EASTERN HEMLOCK.— 
The common hemlock of the eastern United States—or spruce 
pine as it is often called in the South—Tsuga Canadensis, has 
long been known to range farther south in Alabama than in any 
other state. Dr. Charles Mohr knew it in this state only from 
a few localities in Winston County, at altitudes exceeding 800 
feet, where it was probably first made known by Judge T. M. 
Peters about fifty years ago.* In March, 1906, I found it near 
Spruce Pine, in Franklin County,j and in November, IgI1, 
in the northeastern portion of Marion County and at the great_ 
natural bridge in the southwestern part of Winston County.t 

About twelve years ago a friend in Tuscaloosa wrote me that 
he had seen a hemlock tree floating in the Warrior River near that 
place at a time of high water, and wondered where it had come 
from. The nearest known stations for it at that time were in 
Winston County, about 60 miles from Tuscaloosa in a straight 
line and at least 100 by water, but the tributaries of the Warrior 
River there are so small and so rocky that it was hard to believe 
that a tree could have floated all the way and remained recog- 
nizable. The facts set forth below, however, explain how such 
a tree could have reached Tuscaloosa with a much shorter 
journey. 


* See Mohr’s Plant Life of Alabama (1901), pp. 34, 72, 159, 208, 324, 325. 
+ Bull. Torrey Club 33: 524-525. 1906. 
t Geol. Surv. Ala., Monog. 8: 49, 136. 1913. 


199 


On September 2, 1919, with a party of visiting geologists, I 
had a boat ride on the reservoir from which water is pumped to* 
most of the iron furnaces and rolling mills of the Tennessee Coal, 
Iron & Railroad Co. in the vicinity of Birmingham. It was con- 
structed eight or nine years ago by building a dam about 90 
feet high across Village Creek just above the mouth of Venison 
Creek, about three miles southwest of Adamsville, in Jefferson 
County, Alabama, in latitude 33° 34’, and about 500 feet above 
sea-level. This creek is a tributary of the Locust Fork of the 
Warrior River, and the dam is about twelve miles from the river 
by the course of the creek, which flows in a general northwesterly 
direction. 

On the shady side of the reservoir, with a northeasterly .ex- 
posure, and also in the gorge just below the dam, we noticed 
several specimens of the tree in question. I did not have time 
to go down the creek below the dam, but judging from the avail- 
able topographic maps conditions should be favorable for the 
hemlock all the way down to the river. The whole country from 
there to Tuscaloosa is in the Warrior coal field, characterized 
by shaly sandstone of the upper Carboniferous. This creek, 
like several other tributaries of the Locust Fork, takes its rise in 
a limestone valley, but that may have little to do with the oc- 
currence of the hemlock. 

At one point a long-leaf pine, Pinus palustris, was noticed on 
the sunny side of the reservoir directly opposite some of the hem- 
lock and scarcely a stone’s throw away. That pine is common 
on many hills and mountains in Jefferson County, and extends 
inland to the northern part of Walker County,* but this is 
probably the first time that its range has been recorded as over- 
lapping that of Tsuga Canadensis. Incidentally, there seems to 
be a wide gap between the known stations for the latter in Ala- 
bama and those in Georgia and Tennessee, a fact not easily 
explained at present.—ROLAND M. HARKER. 

* See Geol. Surv. Ala., Monog. 8: 54, 140. 1913. 


UNIVERSITY, ALA. 


200 


REVIEWS 


Britton and Rose’s Cactaceae* - 


The recent death of Andrew Carnegie, who lived only a few 
weeks after this volume was issued, recalls the publication of 
Carnegiea gigantea in 1908, when the senior author first associated 
the iron master with the cactus family. To many the assign- 
ment of his name to the giant cactus appeared at that time a 
doubtful compliment either to the cactus or to Mr. Carnegie. 
It is not without interest, then, that the chief agency which he 
set up for the advancement of science should have sought out 
the authors of the present great volume who have abundantly 
justified the wisdom of that association. For the Carnegie 
Institution has issued, and the authors have prepared, the most 
sumptuous botanical publication since Dyke’s ‘‘The genus 
cists 

The book, as was to be expected, deals with the systematic 
botany of the cactus family, but more thoroughly than any other 
as yet issued. The only other work of monographic pretensions 
is Karl Schumann’s Gesamtbeschreibung der Kakteen issued in 
1903. As an illustration of the difference in the volumes, 
Opuntia proper in the new book contains 254 species, in the 
old one, 162. Not all of the increase is due to the newer taxon- 
omy; in fact a surprising amount of it is due to exploration, and 
to the consequent discovery of new kinds of prickly pears. This 
group occupies the major part of the volume, and segregates 
from it, with Pereskia, the whole of it. The extent of the ex- 
ploration, from British Columbia to the Argentine, its com- 
prehensive nature, including hundreds of the islands and keys 
of the West Indies, its personnel which has included nearly all 
the botanists with tropical experience in the United States and 
many of our South American and West Indian neighbors,—this 
has given the authors who have done a tremendous amount of 
exploration themselves, an opportunity for comparative study 


* Britton, N. L. and Rose, J. N. The Cactaceae. Descriptions and Illustra- 
tions of Plants of the Cactus Family. Vol. 1, pp. 1-236. Plates 1-36 (many in 
color), figs. 1-303. Carnegie Institution of Washington, Publication No. 248. 
21 June 1919. Price $18.00. 


201 


of these puzzling plants, that they have used to splendid ad- 
vantage. 

Detailed comment of such a large work is obviously impossible, 
but mention should be made of the scheme the authors have 
followed. ‘There are, of course, keys to the tribes, genera under 
the tribes, and to the series and species where the genera are 
large enough to need such subdivisions. 

For each of the species there is a complete synonymy, and 
where, as in Opuntia, there are 900 names known for about 250 
plants this will be of great value. There follows a description of 
the species, a statement of its type locality and the distribution 
of it. Notes of its variants, its affinities to related species, 
illustration of it and other items, complete the record of the 
treatment. Very nearly all the species are illustrated by photo- 
graphs of mature plants, drawings of significant parts, or by 
colored illustrations of the joints or flowers or fruits. No recent 
botanical work has such a wealth of illustrations, and in such 
plants as the cactus, which exhibit different characters at different 
periods of growth, these are of paramount value in aiding iden- 
tification. | 

The prickly pears, comprising four fifths of the volume, are 
grouped into 3 subgenera and 46 series, the characters of which 
are based on a study of living plants of which the New York 
Botanical Garden and the Department of Agriculture now have 
the largest collections known. Scores of cases of mistaken 
identity, of the description of stages of one species as several, of 
mistaken ideas of distribution and the other hazards due to the 
difficulty of the group and early misconceptions, are now straight- 
ened out. The gardener, field botanist, plant geographer and 
ecologist can now find for the first time an accurate record of the 
species and their distribution. Such a work and its changes 
will produce shocks to the mentally well-intrenched, as for in- 
stance, that the supposedly widely distributed Opuntia tuna is 
actually confined to the lowlands of Jamaica; that O. vulgaris 
Mill. long supposed to be native here-abouts, does not occur in 
North American except as an escape in Cuba, and many other 
errors that have passed current. 


202 


An interesting tabulation could be made by those interested in 
endemism on the number of prickly pears with a relatively 
restricted distribution. Scores have been found only in isolated 
regions, a few scattered through neighboring cactus deserts, 
still fewer of very general distribution in tropical America, of 
which Opuntia ficus-indica seems to be the most ubiquitous.* 
As the group is wholly American, the distribution in North or 
South America, or in the West Indies, plotted out as to the apparent 
centers of distribution of some of the significant species, would be 
of particular interest. Asa partial aid to such an understandin g, 
the reviewer lists the chief cactus regions of the area covered by 
the book with the number of species recorded from there by the 
authors. 


Southwestern United States and adjacent Mexico......... 63 
IMexicoranda Central eAmentcaa see cae 62 
The Argentine, including Paraguay, Uraguay & Chile...... 61 


As between these two great centers of cactus species, for the 
first two are probably inseparable, the links are very few and 
scattered. The authors record only three species that are 
common, as natives, to both regions and are found in the inter- 
vening area. ‘There are, of course, other prickly pears between 
these two great centers as, for instance, 12 in Bolivia, 14 in 
Peru, 9 in Ecuador, 7 in Brazil, 5 in Colombia, and 4 in Venezuela 
and adjacent islands. 

These 56 species, endemics nearly all, and often separated by 
rain forests, seem a somewhat slender thread to stretch across the 
three or four thousand miles between the northern and southern 
culminations of the cactus flora. As a matter of record, the 
figures for the rest of the genus are given herewith. West Indies 
15, Bahamas 4, Tropical America generally 3, Southeastern 
United States 11, Central United States 6, Northeastern United 


* An interesting case of apparent endemism is that of O. Skottsbergii, a species 
described as new in the book. It is native in Santa Cruz territory in the Argentine, 
and, apparently unknown to the authors, was described briefly, it is true, by Skotts- 
berg in his Die Vegetationsverhialtnisse Langs der Cordillera de los Andes, which 
was published on April 26, 1916, in Kungl. Sv. Vetenskapsakademiens Handlingar, 
Band 56, no. 5, at page 268. Dr. Skottsberg credits the species to the authors of 
the present volume, so there is fortunately only a question of priority of publica-- 
tions involved in the case, not another name added to the nine hundred! 


203 


States 1, Galapagos Islands 1. The other genera of the Cac- 
taceae may reveal, when the authors have completed the four. 
volumes which will comprise the work, some further data on 
these problems of distribution. Not the least valuable feature 
of the book is the basis it will furnish for such studies, and in the 
final volume it is to be hoped the authors will include such data. 
Something has recently been issued or spoken about codpera- 
tion in science. This attack upon the problems of the Cac- 
taceae, largely engineered by Messrs. Britton and MacDougal, 
has secured the cooperation of the Carnegie Institution, New 
York Botanical Garden, U. S. National Museum, U. S. De- 
partment of Agriculture, and the Gray Herbarium. Add to this 
hosts of individuals who have contributed notes or specimens 
and it is little wonder that, under the guidance of the authors, 
the book should have grown into incomparably the best one on 


its subject that has yet appeared. 
Was Ee 


NEWS ITEMS. 


Professor Edward W. Berry, of the Johns Hopkins University, 
has returned to Baltimore after six months exploration of the 
Andes of Peru, Bolivia and Chile. 


At the New York Botanical Garden the lectures for the latter 
part of November will be held in the Central Display Green- 
houses at three-fifteen o’clock. They will occupy half an hour, 
will be illustrated by living plants and followed by demonstrations 
in the greenhouses. The dates and subjects are as follows: 

Nov. 15. ‘‘Cycads and Sago Palms,” by Dr. N. [{L. Britton. 

Nov. 22. “Tropical Orchids,” by Mr. Geo. V. Nash. 

Nov. 29. ‘‘ Tropical Ferns and Their Relatives,’’ by Dr. H. 
A. Gleason. 


In a recent flight from Italy to Paris an aeroplane, which was 
carrying as a passenger Mr. Aaron Aaronsohn, was wrecked, 
killing both occupants. Mr. Aaronsohn will be remembered by 
the Club as the director of the Jewish Agricultural Experiment 


204 


Station in Palestine. He lectured at the American Museum of 
Natural History on February 15, 1913, on ‘‘ The story of the 
Wild Wheat and its practical development.”’ 


Professor A. H. Cockayne, a son of Dr. L. Cockayne of Wel- 
lington, New Zealand, is now in the United States, visiting the 
more important botanical institutions. He delivered a lecture 
before the Club on November 11, on ‘‘ Botanical features of the 
flora of New Zealand.” 


In the September number of the Journal of the International 
Garden Club there are two articles of interest to botanists. One 
is Carl Purdy’s ‘‘ Pacific Coast Wild Flowers’”’ which contains a 
wealth of material on the ornamental wild plants of that region 
and a brief history of their earliest collectors. The other is by 
Mrs. Zelia Nuttall of Coyoacan, Mexico, on ‘‘ The Flower lovers 
and gardeners of Ancient Mexico.’”’ While it is an important 
contribution to a rather obscure subject, the author, who has 
lived for years near Mexico City, has written with a delightful 
style that will interest all who enjoy accounts of the early races 
of Americans and their relation to the flowers and plants of the 
country. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six gratuitous copies 
of the number of TORREYA in which thei? papers appear, will kindly notify the 
editor when returning proof. 

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Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs, E. G. BRITTON, Chairman. 
J. H. BARNHART, Pror. JEAN BROADHURST 
Miss C. C, HAYNES B. O. DODGE 
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Budget Committee F. J. SEAVER 
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Field Committee Phanerogams: Cryptogams: 
F. W. PENNELL, Chairman. E. P. BICKNELL Mrs, E.G. BRITTON 
Mrs. L. M. KEELER N. L. BRITTON T. E. HAZEN 
MICHAEL LEVINE C. C. CurRTIS M. A. Howe 
GEORGE T. HASTINGS K. K. MACKENZIE MICHAEL LEVINE 
PErcy WILSON NORMAN TAYLOR W. A. MuRRILL 


F. J. SEAVER 
Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C, Barbour 


Mosses: Mrs, E. G.-Britton Sphaeriaceae, Dothideaceae: H. M. 
Liverworts: A. W. Evans Richards 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W..A. Murrill Imperfecti: H. M. Richards, F,. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhurs 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


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ORREYA 


A Montuiy Journat or Boranicat Notes AnD News 
EDITED FOR 


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CONTENTS 
Scrophulariaceae of the local Flora. IV: F. W. PENNELL --1-s.-s2-6cceeeeete verte: 205 
The Grasses of Salem, Orégon, and Vicinity: J. C. NELSON ..-...-...-+.- BN stg 216 
Wotes on Coelopyne:-T. Di A. CoCKERELL 6.) oie en ek eee teal nse nese eae ees ayo 227 
Book Reviews 
Rock’s Lobelioideae of Hawaii: THe EDITOR ....-.-.. --.-se.seeeesees PEON are 228 
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TORREYA 


Vol. Ig No. I1 
November, IgIg 


SeROPHULARIACEAE OF THE, LOCAL: FLORA... IV 


By FRANCIS W. PENNELL 
(Continued from September TORREYA) 


13. AUREOLARIA Raf. New FI. Amer. 2: 58. 1837 
Type species, A. villosa Raf. 


Annual. Stem, leaves and calyx with stalked or sessile glands. Leaves bipin- 
natifid, more or less pectinately cut. Calyx-lobes dentate to pectinate. 
Corolla externally glandular-pubescent, within pubescent over bases of the 
posterior lobes; more or less marked or tinged with purple-red. Anther-sacs 
2.5-4 mm. long. Capsule ellipsoid, 9-12 mm. long, 1/2—2/3 enclosed in the 
calyx-tube, glandular-puberulent. Seeds .8 mm. long, not winged. Pedicels 
10-28 mm. long. (Panctenis Raf.) 

Stem closely pubescent above, not or scarcely glandular. Leaves puberulent, 
not or slightly glandular. Capsule-narrowly ellipsoid, 9-11 mm. long. 
Leaves 3-6 cm. long. Pedicels mostly 
shorter than to equaling the bracts. 
Stem (frequently) glandular-hirsute be- 
low. I. A. pedicularia. 
Leaves 1.5—2.5 cm. long. Pedicels longer 
than the bracts. Stem not glandular- 
hirsute below. ta. A. pedicularia caesariensis. 
Stem glandular-pubescent above with scat- 
tered glands. Leaves glandular-puberu- 
lent to pubescent. Capsule ellipsoid, 
II—12 mm. long. 1b. A. pedicularia intercedens. 

Perennials. Not glandular. Leaves entire to 
pinnately cut, and slightly bipinnatifid, 
though not pectinate. Corolla externally 
glabrous, within glabrous or diffused-pubes- 
cent; not marked or tinged with red-purple. 

Anther-sacs 4-6 mm. long. Capsule ovate 
to globose-ovate in outline, not enclosed 
within the calyx-tube, not glandular. 
Seeds 1I.5-2.7 mm. long, broadly winged. 


[No. 10, Vol. 19 ot TorREYA, comprising pp. 187-204, was issued Dec. 1, 1919.] 


205 


206 


Pedicels I.5-10 (-I5) mm. long. (Euau- 
reolaria.) 
Capsule densely rusty-pubescent. Stem pubes- 
cent and leaves downy-pubescent. Ped- 
icels 1.5-3 mm. long. 2. A. virginica. 
Capsule glabrous. Stem glabrous and leaves 

glabrous or minutely puberulent on the 
upper surface. Pedicels 3 mm. long or 
longer. 

Stem slender, not glaucous, rarely pur- 
plish. Petioles very short, less than 10 
mm. long.. Lower leaves lanceolate 
to ovate-lanceolate, widest below the 
middle, long-acuminate. Pedicels 3-8 
mm. long. Corolla 30-35 mm. long. 
Seeds 1.5-1.7 mm. long. 3. A. laevigata. 

Stem relatively stout, glaucous, frequently 
purple. Petioles mostly over I0 mm. 
long. Lower leaves ovate-lanceolate 
to ovate, widest about the middle, not 
long-acuminate. Pedicels 5-10 (-15) ~ 
mm. long. Corolla 35-40 mm. long. 
Seeds 2—2.7 mm. long. 4. A. flava. 


1. AUREOLARIA PEDICULARIA (L.) Raf. 

Gerardia pedicularia L. Sp. Pl. 611. 1753. ‘‘Habitat in 
Virginia, Canada.” Type not seen, but description 
sufficiently distinctive. 

Panctenis pedicularia (L.) Raf. New Fl. Amer. 2:61. 1837. 
The specific name spelled by Rafinesque “ pedicularis.”’ 

Aureolaria pedicularia (L.) Raf. l.c. 61. 1837. 

Dasystoma pedicularia (L.). Benth. in DC. Prod. 10: 521. 
1846. 

Agalinis pedicularia (L.) Blake in Rhodora 20: 70. 1918. 

Flowering from early August to late September, fruiting from 
September into November. 

Dry oak-woodland, thin soil, sandy or rocky, occasional or 
local above Fall-line, more frequent southwestward; in the 
Coastal Plain of Long Island and New Jersey, passing into var. 
caesariensis. Northwestward the species passes into var. 
intercedens. Ranges, southward and westward mainly through 
its varieties, from western Maine to North Carolina and Minne- 
sota. 


207 


Ia. AUREOLARIA PEDICULARIA CAESARIENSIS Pennell in Bull. 
Torrey Club 40: 413. 1913. ‘‘Type, Atco, Camden- 
Co., New Jersey, Sept. 7, 1911, F. W. Pennell 3545 in 
Herb. University of Pennsylvania.” 
Sandy open woodland, Coastal Plain of Long Island and New 
Jersey, mainly in the Pine Barrens, where it replaces the species. 
Occurs northeastward to southeastern Massachusetts. 


1). Aureolaria pedicularia intercedens Pennell, var. nov. 

Stem glandular-pubescent above, with spreading or recurved 
short hairs, scattered among which occur glands which are 
borne on stalks shorter than or longer than the pubescence. 
Leaves somewhat puberulent with short-stalked glands. Calyx- 
lobes 8-13 mm. long. Capsule 11-12 mm. long. Otherwise as 
in the species. 

Type, Mt. Arlington, Morris Co., New Jersey, collected in 
flower August 26, 1906, K. K. Mackenzie 2356; in Herb. Missouri 
Botanical Garden. 

Environment of the species, between which and the densely 
hirsute western A. pedicularia ambigens (Fernald) Farwell it 
forms a connected series of intergradations. Occasional in 
northern New Jersey and eastern Pennsylvania, to be expected 
with the species in our northwestern counties in New York. 


2. AUREOLARIA VIRGINICA (L.) Pennell. 

Rhinanthus virginicus L. Sp. Pl. 603. 1753. ‘‘Habitatin Vir- 
ginia.’’ As specimen in the Linnean Herbarium bears the 
handwriting of Linné the younger and so appears to have 
been a late addition, Gronovius’s plant must be taken as 
the type. This is Clayton 488, recently identified by 
Dr. S. F. Blake, in Rhodora 20: 66. 1918, as the plant 
here considered. Our traditional applications of the 
names virginica and flava must be transposed. 

Aureolaria villosa Raf. New Fl. Amer. 2: 59. 1837. No 
type locality given, nor type known to exist. Description 
sufficiently distinctive. 

Dasystoma pubescens Benth. in DC. Prod. 10: 520. 1846. 
“In Americae sept. civitatibus orientalibus frequens.” 
Type not verified, but description sufficiently distinctive. 


208 


Gerardia virginica (L.) Britton in Prelim. Cat. N. J. Pl. 40. 


1888. 

Dasystoma virginica (L.) Britton in Mem. Torr. Bot. Club 5: 
295. 1894. 

Aureolaria virginica (L.) Pennell in Bull. Torr. Bot. Club 
40: 409. I913. 


Agalinis virginica (L.) Blake in Rhodora 20: 71. 1918. 

Flowering from early July to mid-August, fruiting from August 
to October. 3 

Dry open oak-woods, usually sand or a sandy loam, frequent 
or common throughout our area, less general within the Pine 
Barrens. Ranges from New Hampshire to Florida, west to 
Michigan, Kentucky and Louisiana. 


3. AUREOLARIA LAEVIGATA (Raf.) Raf. 

Gerardia levigata Raf. Ann. Nat. 13. 1820. “It grows 
on the knob hills of Kentucky, the Cumberland mountains: 
and the Alleghany.’’ No type known to exist, unless it 
be a specimen in Herb. New York Botanical Garden, 
labeled in Rafinesque’s handwriting, ‘‘Gerardia—n. sp.— 
Kentucky.”’ 

Aureolaria levigata (Raf.) Raf. New Fl. Amer. 2:59. 1837. 

Dasystoma laevigata (Raf.) Chapm. FI. S. Un. St. ed. II: 
636. 1883. 

Agalinis laevigata (Raf.) Blake in Rhodora 20: 71. 1918. 

Oak-woodland, usually rocky, along streams or on mountain- 
sides along the Susquehanna River in Lancaster Co., Pennsyl- 
vania. Ranges through the Appalachians from central Pennsyl- 
vania to South Carolina and Tennessee. 


4. AUREOLARIA FLAVA (L.) Farwell. 

Gerardia flava L. Sp. Pl. 610. 1753. ‘Habitat in Virginia, 
Canada.”’ Specimen in Linnean Herbarium identified 
by Bentham; see in Comp. Bot. Mag. 1: 198. 1836. 

Gerardia glauca Eddy in Med. Repos. N. Y., IInd Hex. 5: 
126. 1807. Plandome, Long Island? Ci We gam 
Type not seen nor known to exist, but description quite 
distinctive. 


209 


Gerardia quercifolia Pursh, Fl. Amer. Sept. 423. 1814. 
“On the banks of rivers, in rich shady places, Pensyl- 
vania to Carolina.” Type not seen, but description 
distinctive. 

Aureolaria glauca (Eddy) Raf. New FI. Amer. 2:60. 1837. 

Dasystoma quercifolia (Pursh) Benth. in DC. Prod. 10: 520. 
18406. 

Dasystoma flava (L.) Wood, Class-Book 529. 1861.. As to 
synonymy, not description, the latter applying to Awreo- 
laria virginica. 

Agalinis glauca (Eddy) Blake in Rhodora 20: 71. 1918. 

Aureolaria flava (L.) Farwell in Rep. Mich. Acad. Sci. 20: 
188. 1918. 

Flowering from late August to late September, fruiting from 
September to November. 

Dry to rather moist oak-woodland, usually on rocky hillsides, 
loam or sometimes in sandy soil, frequent or locally common 
through the counties above the Fall-line, especially toward the 
mountains; on northern Long Island, but rare in southern Long 
Island and very rare in the Coastal Plaimof New Jersey. In- 
cluding varieties, this species ranges from Maine to Florida, 
Illinois, Arkansas and Louisiana. 


14. AGALINIS Raf. New FI. Amer. 2:61. 1837 
Type species, A. palustris Raf. 


Corolla with lobes all spreading, pubescent within at base of posterior lobes. 
Seeds dark-brown. Plants tending to blacken in drying. Calyx-tube not 
evidently reticulate-venose. 

Pedicels less than 12 mm. long. Inflorescence of normal racemes. Seed- 
coat with dark-brown ridges, between which are broad areas, paler 
and minutely reticulate. 

Leaves and calyx-lobes obtuse to acutish. Anther- 

sacs obtuse to acutish. Plant fleshy, bushy- 

branched below, with elongated racemes above. 

Pedicels 5-12 mm. long. Corolla 12-17 mm. 

long. 1. A. maritima. 
Leaves and calyx-lobes acute to acuminate. Anther- 

sacs mucronate to minutely awned. Plants not 

fleshy, more uniformly branched. Pedicels 

rarely over 5 mm. long. 


210 


Calyx-lobes 4/5-7/8 the length of the tube, tri- 
angular-lanceolate to lanceolate. Corolla 
12-20 (—23) mm. long. Stem 1-6 dm. tall. 
Anther-sacs somewhat pubescent to glab- 
rous. 

Calyx-lobes 1/6-1/2 the length of the tube, tri- 
angular-lanceolate to subulate. Corolla 20— 
38 mm. long. Stem 3-12 dm. tall. An- 
ther-sacs densely lanate. 

Stem relatively stiffly branched, sparingly 
scabrellous. Calyx-lobes triangular-lanceo- 
late to subulate. Corolla 20-38 mm. long. 
Leaves linear, I-3 mm. wide. 

Stem slender, virgately branched, glabrous. 
Calyx-lobes triangular-subulate to subulate. 
Corolla 20-25 mm. long. Leaves narrowly 
linear to almost filiform, .5—1 mm. wide. 

Pedicels 15-40 mm. long. Inflorescence a short raceme, 


one pedicel (by arrested growth of the rhachis) 


appearing terminal. Seed-coat with dark-brown 
ridges, between which are narrow scarcely paler 
areas. Corolla 18-25 mm. long. Leaves narrowly 
linear to filiform. 

Seeds yellowish-brown. Plants scarcely tending to blacken 
in drying. Calyx-tube evidently reticulate-venose. 
Corolla 13-15 mm* long. 

Calyx-tube campanulate, 3 mm. long, firmer in texture, 
2/3-3/4 the length of the capsule, its lobes .5-I mm. 
long, triangular-acuminate, not or scarcely callose. 
Seeds .4—.6 mm. long, strongly reticulate. Pedicels 
mostly I-2 times the length of the bracts. Stem 
usually 1-4 dm. tall. 

Calyx-tube hemispheric, 2.5-3 mm. long, thinner in tex- 
ture, 3/5-2/3 the length of the capsule, its lobes 
minute, .05—.2 (-.3) mm. long, strongly callose. Seeds 
.6—.8 mm. long, obscurely reticulate. Pedicels mostly 
2-3 times the length of the bracts. Stem usually 2-5 
dm. tall. 

Corolla with the posterior lobes ascending-arched over- the 
stamens and style, glabrous within at base of the posterior 
lobes. Racemes elongated, normal. Pedicels 12-27 mm. 
long. Seeds dark-brown. 


1. AGALINIS MARITIMA (Raf.) Raf. 


Gerardia maritima Raf. in Med. Repos. N. Y., 


2. A. paupercula. 


3. A. purpurea. 


4. A. virgata. 


5. A. Holmiana. 


6. A. acuta. 


7. A. decemloba. 


8. A. tenuifolia. 


IInd Hexr3: 


361. 1808. ‘‘Found in the islands of Egg-Harbour, in 
New Jersey.”’ No type known to exist, but description 


211 


quite distinctive. An unpublished plate of Rafinesque’s 
is in the library of the New York Botanical Garden. 
Gerardia purpurea crassifolia Pursh, Fl. Amer. Sept. 422. 
1814. ‘‘In salt marshes, near New York.” Type not 
seen, but description sufficiently distinctive. 
Agalinis maritima (Raf.) Raf. New Fl. Amer. 2:62. 1837. 

Flowering from mid-July to early September, fruiting Sep- 
tember to October. 

Salt marshes, along the Atlantic coast, Connecticut, New 
York and New Jersey. If separable from the much larger plant 
of the Southern and Gulf coast, our species ranges from Virginia 
northward to Maine, becoming progressively smaller and simpler 
northward. 


2. AGALINIS PAUPERCULA (A. Gray) Britton. 

Gerardia purpurea paupercula A. Gray, Syn. Fl. N. Amer. 
II. r: 293. 1878. “‘Lower Canada to Saskatchewan 
and southward from coast of New England to Penn., 
N. Illinois and Wisconsin.’’ Numerous specimens labeled 
by Gray seen, but none indicated as typical. In synon- 
ymy is mentioned the name intermedia Porter in herb., 
-so selecting a type. 

Gerardia paupercula (A. Gray) Britton in Mem. Torr. Bot. 
Club 5: 295. 1894. 

Agalinis paupercula (A. Gray) Britton in Britton & Brown, 
Ill. Fl. ed. II. 3: 210. 1913. . 

Flowering from early August to September, fruiting September 

to October. . 
Moist soil, borders of lakes and in bogs, especially where 
sandy, in the glaciated region; through the area east of the Hud- 
son River, occasional in Connecticut and northward in New 
York, very rare southward and on Long Island only at Lake 
Ronkonkoma; near Dingmans Ferry, Sussex Co., New Jersey 
(W. M. Van Sickle (E) ), and doubtless occasional elsewhere in 
the glaciated region west of the Hudson, especially in New York. 
Ranges through glacial bog country from New Brunswick to 
Minnesota, but seems to be much more common in northern 
New England and in Michigan than through the intervening 


212 


area. Along their lines of contact in southern New England, 
our area and in northern Indiana and Illinois, this intergrades 
somewhat with its obvious parent, A. purpurea. 

3. AGALINIS PURPUREA (L.) Pennell. 

Gerardia purpurea L. Sp. Pl. 610. 1753. ‘Habitat in 
Virginia, Canada.’ The Linnean diagnosis includes 
both long and short-pediceled plants, so could include all 
pink (=“‘purple’’) flowered species. The first citation 
accompanied by a figure, Plukenet’s “ Digitalis virginiana 

evidently the 
prevalent plant of the Atlantic seaboard now under 


7 


rubra, folis & facie Antirrhini vulgaris, 


consideration, is counted as the type. 

Gerardia purpurea grandiflora Benth. in Comp. Bot. Mag. 1: 
208. 1836. ‘Hab. New Jersey.’’ Type, labeled “New 
Jersey, Torrey 1834,’ seen in Kew Herbarium. 

Agalinis palustris Raf. New Fl. Amer. 2:62. 1837. ~ Near 
marshes .. . . From New England to Carolina.” Type 
not known to exist. Evidently intended for the prevalent 
plant of the Atlantic seaboard. ; 

Agalinis longifolia Raf. |.c. 62. 1837. “Near streams New 
Jersey to Virginia.”’ Type not known toexist. Asmaller 
form. 

Gerardia furpurea f. albiflora Britton in Bull. Torr. Bot. Club 
17: 125. 1890. New Jersey. An albino state. Plants 
with pure white corollas are occasional in any species of 


this genus. 
Gerardia purpurea parvula Pennell in Proc. Acad. Nat. Sci. 
Phila. 62: 572. I911. ‘‘Serpentine, Wawa, Delaware 


county, Penna., Ff. W. Pennell 2689, coll. Sept. 25, 
1910, in Herb. Acad. Nat. Sci. of Phila.” The-smaller- 
flowered depauperate plant characteristic of the Serpen- 
tine Barrens. 

Agalinis purpurea (L.) Pennell in Bull. Torr. Bot. Club 40: 
£26... LOTS. 

Aureolaria purpurea (L.) Farwell in Rep. Mich. Acad. 
Sci. 20: 189. 1918. 

Flowering from late August to mid-September, fruiting Sep- 

tember to October. 


213 


Moist sandy soil, edges of salt-marsh, of lakes, or of rivers, 
in depressions among sand-dunes, or locally on barren magnesian 
loam in the Serpentine; abundant through the Coastal Plain of 
New Jersey and common in southern Long Island, in the Pine- 
Barrens replaced by A. virgata; above the Fall-line occasional 
near ponds and bogs of northern New Jersey, in the bogs of 
Lancaster Co., Pennsylvania, and in meadows and on dry 
grassy upland of the Serpentine Barrens of Delaware and Chester 
counties, Pennsylvania. Ranges from Massachusetts to Florida, 
Minnesota and Texas, mainly in the Coastal Plain or at low 
elevations inland. 


4. AGALINIS VIRGATA Raf. New FI, Amer. 2: 62. 1837. “Glades 
of Pine woods in South New Jersey near Mullica Hill, &c.”’ 
Type not known to exist. 
Gerardia racemulosa Pennell in Torreya II: 15. I9I11I. 
““Type—Parkdale, Camden Co., N. J., #. W. Pennell 
2692 Coll. Sept. 27, 1910, in Herb. Acad. Nat. Sci. of 
Phila.” 

Flowering from September to mid-October, fruiting slightly 
later. 

Moist sandy pine-barrens, or occasionally in open sand, in the 
Pine Barrens of Long Island (Great River, Suffolk Co., E. P. 
Bicknell) and of southern New Jersey. Ranges from Long 
Island to South Carolina, in the pine barrens of the Coastal 
Plain. An obvious derivative of A. purpurea. 


5. AGALINIS HOLMIANA (Greene) Pennell. 

Gerardia Holmiana Greene, Pittonia 4:52. 1899. “‘Plentiful 
in open pine and oak groves along Michigan Avenue 
south of the Soldiers’ Home grounds near Brookland, 
D. C., collected by Mr. Holm and the writer, 20 Oct., 
1898.’’ No specimen of this date seen, but one in the 
herbarium of the New York Botanical Garden, of Dr. 
Greene’s collecting, from Brookland, D. C., dated Oct. 
16, 1898, may stand as the type. I have collected this 
plant at the type station. 

Agalinis Holmiana (Greene) Pennell in Bull. Torr. Bot. 
Club 40: 429. I913. 


214 


Flowering early September to mid-October, fruiting slightly 
later. ; 

Dry sandy pine-land, in the Coastal Plain. Occasional on 
Long Island, and common through the Pine Barrens of southern 
New Jersey. Ranges from Long Island to Alabama, through 
the Coastal Plain. 


6. AGALINIS ACUTA Pennell in Bull. Torr. Bot..Club 42: 338. 
1915. “‘Type: dry sandy downs, Edgartown, Martha’s 
Vineyard, Massachusetts, collected. in flower September 
12, 1901, M. L. Fernald 45 in United States National 
Herbarium.” 

Flowering from late ae to mid-September, fruiting Sep- 
tember to October. 

Dry sandy soil, sterile sandy loam, local in the Coastal Plain 
of Long Island, and known inland from Farmington, Hartford 
Co., Connecticut (Bissell 14, 48, 439). Abundant on the Hemp- 
stead Plains of Long Island, one of the most distinctive plants 
of that prairie. 


7. AGALINIS DECEMLOBA (Greene) Pennell. 

Gerardia decemloba Greene, Pittonia 4: 51. 1899. “Plant 
not uncommon about Brookland, D. C., inhabiting grassy 
knolls and hillsides bordering on pine woods.” <A speci- 
men in herb. New York Botanical Garden, collected by 
Dr. E. L. Greene at Brookland, D. C. in Oct., 1898, may 
stand as the type. 

Agalinis decemloba (Greene) Pennell in Bull. Torr. Bot. 
Club 40: 434. 1913. 

Flowering from early September into October, fruiting late 
September an October. 

Dry soil, sand or clay, in our area only in southern Lancaster 
Co., Pennsylvania. (New Texas and Wakefield.) Ranges from 
thence southwestward to northern Alabama, but with a distri- 
bution much broken, though, like the last, locally common. 


8. AGALINIS TENUIFOLIA (Vahl) Raf. 
Gerardia tenuifolia Vahl, Symb. Bot. 3:7. 1794. ‘Habitat 
in America septentrionali.”” Type in Herb. Universi- 


tetets Botaniske Museum, Copenhagen, Denmark, col- 
lected by Von Rohren, and said to be probably frorm 
Philadelphia, is identified by Dr. C.-H. Ostenfeld as 
identical with my number 2687 from Secane, Delaware Co., 
Pennsylvania. 

Agalinis tenuifolia (Vahl) Raf. New Fl. Amer. 2:64. 1837. 

Gerardia tenutfolia f. albiflora Britton in Bull. Torr. Bot. 
Club 17: 125. 1890. ‘‘Found by Mr. Leggett at South 
Amboy, and by Mr. Schuh at Rosemont, [New Jersey].”’ 
An albino state. 

Aureolaria tenuifolia (Vahl) Farwell in Rep. Mich. Acad. 
Sek 207189.) LOTS: 

Aureolaria tenutfolia albiflora (Britton) Farwell, l|.c. 190. 
1918. | 

Flowering from late August to early October, fruiting Sep- 
tember and October. 

Dry loam, or at times sandy soil, usually in open deciduous 
woodland, common throughout the area above the Fall-line; on 
northern Long Island; in the Coastal Plain of Long Island and 
New Jersey occasional, or frequent in heavy soils, not in the 
Pine Barrens. Ranges from Maine to Georgia, Louisiana, 
Michigan and Missouri, and in its varieties westward to North 
Dakota, Colorado and Texas. 


15. OTOPHYLLA Benth. in DC. Prod. 10: 512. 1846 
Type species, Gerardia auriculata Michx. 

(?) Tomanthera Raf., New Fl. Amer. 2: 65. 1837. Type 
species, T. lanceolata Raf. 

I. OTOPHYLLA AURICULATA (Michx.) Small. 

Gerardia auriculata Michx. Fl. Bor. Amer. 2: 20. 1803. 
“In pratis regionis Illinoensis.’”” Type not verified, but 
description sufficiently distinctive. 

Seymeria auriculata (Michx.) Spreng. Syst. 2: 810. 1825. 

(2) Tomanthera lanceolata Raf. New Fl. Amer. 2:66. 1837. 
‘““My specimen of Collins’ herbarium was collected by 
Dr. Cleaver in New Jersey.’’ The description of this is 
erroneous for our plant in describing the anther-sacs as 


216 


* 


unequal; actually they are alike in each stamen but those 
of the posterior stamens are smaller. However I am 
convinced that ours must be the plant of Rafinesque, and 
that such an error is due either to a lapse of memory in 
recording his observation or more likely to confusing in 
his dried specimen the sacs of two different stamens. 
This opinion is confirmed by Rafinesque’s inclusion in - 
his new genus of Michaux’s plant. However for anything 
less than a certainty and for an untrue name it may be 
unwise to dispossess Bentham’s well-chosen name. 

Tomanthera auriculata (Michx.) Raf. 1. c. 66. 1837. 

Otophylla Michauxit Benth. in DC. Prod. Io: 512. 1846. 
New name for Gerardia auriculata Michx. _ 

Otophylla auriculata (Michx.) Small, Fl. S.E. Un. St. 1075, 


1338. 1903. 
Agalinis auriculata (Michx.) Blake in Rhodora 20: 71. 
1918. 


Aureolaria auriculata (Michx.) Farwell in Rep. Mich. 
Acad: Stl 20; 180. A918: 

Flowering from late August to mid-September, fruiting Sep- 
tember and October. 

‘Old fields and railway banks, occasional in New Jersey and 
Pennsylvania. Certainly introduced from the prairies of the 
Mississippi Valley states. 

(To be conciuded.) 


THE GRASSES OF SALEM, OREGON AND VICINITY 
By JAMES C. NELSON 


The following list represents the result of five seasons’ col- 
lecting in the general region adjacent to Salem. Although the 
work has been done in the all-too-brief moments that could be 
snatched from arduous professional duties, and makes no claim: 
to completeness, the writer ventures to believe that most of the 
grasses growing spontaneously in the territory under consider- 
ation have been included. In the case of the introduced species, 
there is the constant possibility of the establishment of new 


217 


forms, which make themselves at home here with surprising 
facility. 

The area covered includes the city of Salem and that part of 
the Willamette Valley in Marion and Polk Counties contiguous 
to the city, extending to the foothills of the Cascades on the 
east and those of the Coast Range on the west, and up to an 
elevation of perhaps 1,000 feet. The Santiam River may be 
regarded as the boundary to the south, and no collections have 
been made more than ten miles north of Salem. No attempt 
was made to reach the grasses of higher elevations. A number 
of mountain species would be added by a survey of the subalpine 
and alpine zones of the Cascades. 

The Willamette Valley in this part of its course is in general 
a wide alluvial plain, lying not more than 200 feet above sea- 
level, with very slight undulations of surface. From the foot- 
hills on the east to those on the west the average width of the 
valley is about 25 miles. The greater part of the area is under 
intensive cultivation. Hops and grain were formerly the chief 
crops, but fruit-growing is rapidly becoming the leading industry. 

Immediately south of Salem a range of hills, known on the 
west side of the Willamette as the Eola Hills, with a maximum 
elevation of about I,100 feet, crosses the valley from southeast 
to northwest. This range seems to represent a very recent geo- 
logic upthrust, and the basaltic rocks which form its core are 
heavily charged with iron, giving to the soil a characteristic red 
tinge. The Willamette River seems to have originally made 
its way through these hills along the valley now followed by the 
Southern Pacific Railway from Jefferson to Salem, and later to 
have been diverted into the present channel, which has cut a 
deep gorge through the hills north of Independence. The soil 
along this old riverbed is made up of stratified boulders and gravel, 
with a comparatively small admixture of sand and loam. In 
other parts of the valley there is a subsoil of tough yellow clay 
overlaid by a rich friable loam, in many places beginning to 
show exhaustion after seventy years of continuous cultivation. 
Numerous small streams traverse the area, Mill Creek being 
the most considerable. These are fringed with a heavy growth 


218 


of ash, dogwood, alder, willow, and other low shrubs. On the 
lighter gravelly soils, Quercus Garryana is the prevailing tree. 
Many fine groves of the ‘Douglas fir” (Pseudotsuga taxtfolia) 
still exist in the level areas, and cover the steeper slopes of the 
foothills. 

The climate is more oceanic than continental in character. 
There are two sharply contrasted seasonal periods. During the 
autumn, winter and spring months, the rainfall is heavy, some- 
times as much as 14 inches in a single month, with a minimum 
winter temperature of not below 20 degrees Fahrenheit. The 
summer on the other hand is almost rainless, and temperatures 
of 100 degrees are not unknown. During the long dry season 
the porous soil becomes thoroughly desiccated, and all herbaceous 
vegetation not under cultivation, with the exception of a few 
drought-resisting plants and those along the streams, is dried up. 
On the setting in of the fall rains, however, the vegetation 
speedily revives, and continues green and luxuriant during the 
mild winter, reaching its maximum development in May and 
June. These conditions make it very difficult for any of the 
introduced pasture-grasses to survive the summer; and while a 
few of the native species seem better adapted to the arid environ- 
ment, little attention has hitherto been given them. _ 

No comprehensive attempt to catalogue the grasses of this 
region seems to have been made. This will be evident from the 
number of species included in the following list which have not 
found mention in any of the published manuals dealing with the 
flora of Western Oregon. These species are marked “‘X.” 
Introduced species are designated by an asterisk (*). The 
nomenclature conforms to that used in A. S. Hitchcock’s treat- 
ment of the Gramineae in Jepson’s Flora of California (1: 82-189. 
1912). The writer is under obligation to Professor Hitchcock 
and Mrs. Agnes Chase for their kindness in examining and verify- 
ing practically all of his specimens. Professor C. V. Piper has 
kindly placed the results of his long and careful study of the 
flora of the Northwest at my disposal; and Professor M. E. 
Peck of Willamette University, who is probably more thoroughly 
conversant with the flora of Oregon than any other Western 


219 


botanist, has very generously contributed the results of his own 
collection and study. Specimens of practically all these grasses 
may be found in the herbarium of Willamette University at 
Salem, and many of them have also been deposited in the Gray 
and the National Herbaria. 


Er. 


10. 


BL. 


i2: 


13. 


*Digitaria humifusa Pers. Not uncommon on sand-bars 
along the Willamette River, and beginning to appear on 
lawns about Salem (X). 


. *Echinochloa crus-galli (L.) Beauv. Not infrequent along 


ditches and in low ground, and occasional in cultivated 
fields. 


. *Setaria viridis (L.) Beauv. An occasional specimen is 


found in cultivated ground and along railroad tracks, 
but it is still to be regarded as a stray in this district. 

Paspalum distichum L. Common on muddy and sandy 
shores of the Willamette about Salem, and apparently 
indigenous, although far out of its ordinary range. 

Panicum barbipulvinatum Nash. Common on river-shores, 
and occasional in sandy fields. Formerly referred to 
P. capillare L., with which it seems to intergrade. 

Panicum Scribnerianum Nash. Not infrequent in dry 
soil, especially where sand or gravel predominates. 


. Panicum pacificum Hitche. & Chase. On gravelly prairies 


about Salem, and more frequent toward the mountains. 

* Panicum miliaceum L. An occasional waif on rubbish- 
heaps about Salem (X). 

Leersia oryzoides (L.) Sw. Along slow streams and on 
muddy rivershores, sometimes forming extensive colonies. 

* Phalaris arundinacea L. Occasional in waste places 
about Salem. The var. picta L. is not uncommon in 
cultivation. 

* Phalaris canariensis L. A waif on rubbish-heaps about 
the State Prison, Salem. 

* Anthoxanthum odoratum L. Not infrequent in pastures 
and on lawns, appearing very early in spring. 

* Anthoxanthum Puelii Lecoq & Lamotte. Occasionally 
found in dry alkaline soil along the road-side. It has 
probably been taken for the preceding (X). 


14. 


15. 


16. 


rife 


18. 


19. 


20. 


Bite 


23. 


24. 


25. 


26. 


28. 


220 


Hierochloe macrophylla Thurb. In rich woods in the foot- 
hills both of the Cascades and the Coast Range. 

Stipa Lemmoni (Vasey) Scribn. On dry rocky hillsides on the 
Eola Hills in Polk County, where it is locally abundant. 
* Phleum pratense L. Oc¢asionally cultivated, and fre- 
quently running wild along roadsides and borders of 

fields. 

* Polypogon monspeliensis (L.) Desf. In ditches and low 
ground especially in alkaline soil. Not common. 

Alopecurus aristulatus Michx. Very common in wet places 
and borders of ponds. The nomenclature of this species 
is much confused. 

* Alopecurus pratensis L. Found only in one station, along 
the S. P. tracks about a mile south of Salem, where it is 
well established. 

* Aristida oligantha Michx. In dry sandy soil and on 
sand-bars along the Willamette, evidently a recent 
introduction from the south (X). 

* Apera spica-venti (L.) Beauv. .A single specimen was 
found on a lawn of Poa pratensis in Salem (X). 


. * Agrostis alba L. Very common along roadsides and in 


pastures. The form known as “creeping bent” (A. 
stolonifera auth. not L.) is common on lawns in Salem. 

Agrostis Hallii Vasey. Not infrequent on dry banks and 
borders of woods. 

Agrostis foliosa Vasey. A grass of the seashore and moun- 
tains, but following the Santiam River down to an eleva- 
tion of over not 600 feet. 

Agrostis microphylla Steud. Very common in ditches and 
low ground, and extremely variable. 

Agrostis hyemalis (Walt.) BSP. Rarely found outside of 
mountain districts, but occasional along streams at low 
altitudes. 


. Agrostis oregonensis Vasey. In marshes in the old bed of 


Lake Labish, east of Brooks. 

* Notholcus lanatus (L.) Nash. Abundantly cultivated 
throughout our range, although of comparatively little 
value, and escaping freely to fields and roadsides. 


45. 


46. 


221 


. * Arrhenatherum elatius (L.) Beauv. Common in dry 


fields and on roadsides, and spreading rapidly. 


. * Atra caryophyllea L. Abundant everywhere in dry or 


rocky sterile soil. 


. * Aira praecox L. Common in a tract of waste ground east 


of the S. P. station at Salem, but not observed elsewhere. 


. * Aira capillaris Host. On sandbars in the North Santiam 


River at North Santiam Station, and also in flower-beds 
on the campus of Willamette University at Salem (X). 


. Danthonia californica Boland. In open meadows, scarce 


in our limits, but becoming more common southward. 


. Danthonia americana Scribn. Very common in dry 


meadows. 


. * Avena fatua L. Introduced along railroad-tracks and 


in waste places (X). 


. * Avena fatua L. var. glabrata Peterm. With the last, but 


more common. 


. * Avena barbata Brot. Frequent along the S. P. tracks 


south of Salem—probably a recent introduction (X). 


. * Avena sativa L. A very common escape along railroad 


tracks and in waste places. 


. Deschampsia caespitosa (L.) Beauv. A very handsome and 


variable grass, common in low ground, especially in 
roadside ditches. 


. Deschampsia danthontoides (Trin.) Munro. Common on 


sand-bars and in dried-up pools along roadsides. 


. Deschampsia elongata (Hook.) Munro. Common on the 


borders of woods and in roadside ditches. 


. Trisetum cernuum Trin. Infrequent in low woods. 
. Trisetum canescens Buckl. Occasional in dry open wood- 


lands. 


. *Gynerium argenteum Nees. Although this shows no 


disposition to spread, it has persisted for years in vacant 
lots where dwellings once stood (X). 

Eragrostis hypnoides (Lam.) BSP. Very common on muddy 
shores of the Willamette River. 

* Cynosurus cristatus L. Occasional on lawns and street- 
parking about Salem. 


222, 


. * Koeleria cristata (L.) Pers. Rather scarce in dry gravelly 


soil. 


. Pleuropogon refractus (Gray) Benth. Along streams in moist 


woods in the foothills, not common. 


. Melica subulata (Griseb.) Scribn. In open rocky woods, 


common. Flowers very early. 


. Melica Geyeri Munro. Occasional on roadsides near 


Salem—probably its extreme northern extension (X). 


. * Briza minor L. Weil established in the State Fair Grounds 


at Salem. Probably introduced from Southern Oregon, 
where it is very common (X). 3 


. Bromus carinatus Hook. & Arn. Very common in dry soil 


everywhere, and probably often confused with the next. 


. Bromus marginatus Nees. In dry open places, especially 


near dwellings, very common. 


. Bromus polyanthus Scribn. In waste-places and on street- 


parkings about Salem, appearing as if introduced (X). 


. Bromus vulgaris (Hook.) Shear. Common in dry open 


woods. A difficult species, very variously understood by 
Western authors. 


. Bromus vulgaris (Hook.) Shear var. eximius Shear. With 


the last, but less frequent. 


. * Bromus tectorum L. Becoming common along railroad- 


tracks and in waste places (X). 


. * Bromus tectorum L. var. nudus Klett & Richter. With 


the last, but much less common. 


. * Bromus villosus Forsk. Becoming very common along 


the railroads and in waste places, and threatening to 
become a serious menace if not checked. 


. * Bromus rubens L. An occasional specimen is found along 


’ railroad tracks. 


. * Bromus sterilis L. Very common in dry sterile soil. 
2. * Bromus hordeaceus L. Perhaps our most common grass— 


abundant in dry soil everywhere, and very variable. 


. * Bromus hordeaceus L. var. leptostachys Beck. In similar 


situations with the last, but not so common. 


. * Bromus secalinus L. Not uncommon in_ grain-fields, 


and occasionally cultivated. 


65. 


76. 


77: 


78. 


223 


* Dactylis glomerata L. A very common escape to fields 
and roadsides. 7 


. * Poa annua L. Extremely common along waysides, in 


cultivated fields and in lawns. Flowers almost continu- 
ously throughout the year. 


. * Poa compressa L. Not infrequent in sandy soil, 


along the Willamette. 


. * Poa pratensis L. Our commonest lawn-grass, and 


escaped to meadows and pastures everywhere. 


. Poa nervosa (Hook.) Vasey. A mountain species that 


has been found in our limits only at Silver Creek Falls in 
the Cascades, on moist rocky banks. 


. * Poa trivialis L. -Not infrequent in damp shady places. 
. Poa triflora Gilib. Common along streams in low ground. 
. Poa leptocoma Trin. In damp thickets at Silver Creek 


Falls. 


. Poa scabrella (Thurb.) Benth. Not infrequent in dry 


gravelly soil about Salem (X). 


. Poa Howellii Vasey & Scribn. Not uncommon in dry 


coniferous woods. 


. Poa multnomae Piper. A grass of the Columbia Gorge, 


but collected on rocks in the bed of Silver Creek, one mile 
above Silverton (X). 

Festuca octoflora Walt. Rather scarce in dry open places 
near the Willamette. 

Festuca megalura Nutt. Very abundant in dry soil along 
roads and in waste places everywhere, appearing as if 
introduced. ? 

* Festuca myuros L. Has been found only at one station, 
on railroad tracks at West Salem, Polk County. 


. * Festuca bromoides L. Occasional along roadsides and 


railroad tracks. 


. Festuca californica Vasey. On dry hillsides at Eola, Polk 


County, not observed elsewhere. 


. * Festuca rubra L. Occasional on lawns about Salem, 


where plainly introduced; but the form on gravelly prairies 
appears to be native. 


89. 


9o. 


96. 


224 


. * Festuca rubra L. var. megastachys Gaudin. Occasional 


along railroad tracks (X). 


. Festuca occidentalis Hook. Not uncommon in dry open 


woods. 


. * Festuca elatior L. Common on roadsides and borders of 


fields. 


. Festuca subulata Trin. In open thickets and borders of 


woods. A species of very rapid growth, often reaching 
a height of 5-6 feet after the first warm days of spring. 


. Festuca idahoensis Elmer. Occasional in dry gravelly soil 


(0.68 : 


; * Scleropoa vrigida Griseb. Around old buildings in the 


business district of Salem (X). 


. Phragmites communis Trin. In swampy soil in the old bed 


of Lake Labish, two miles east of Brooks (X). 

Glyceria leptostachya Buckl. Borders of ponds and slow 
streams, not common. 

Glyceria occidentalis (Piper) comb. nov. First described as 
Panicularia occidentalis in Piper & Beattie, Fl. N. W. Coast 
59 (1915). It was originally collected by Hall in the. 
vicinity of Salem, where it is not infrequent along. wet 
ditches. Easily distinguished from G. leptostachya by 
the acutish lemmas. So far as I know it has not yet been 
transferred to Glyceria, and the combination is accordingly 
proposed. / 


. Glyceria pauciflora Presl. Common along streams and in 


wet places. 


. Glyceria grandis Wats. With the last, but less common. 
. Beckmannia erucaeformis (L.) Host. In ditches and wet 


meadows, not common. 


. * Lolium temulentum L. Rather scarce, but occasionally 


too abundant in grain fields. 


. * Lolium multiflorum Lam. Abundant in dry soil almost 


everywhere. Apparently long confused with the next. 

The species is very subject to teratological variations. 

An apparent hybrid with Festuca elatior has been collected. 
* Lolium perenne L. With the last, but less common. 


97. * Lolium perenne L. var. cristatum Doell. <A single speci- 
men was collected in a wooded ravine near Eola, Polk 
County, at considerable distance from any dwelling or 
cultivated ground. 

98. Agropyron tenerum Vasey. Not uncommon in dry soil in 
meadows and grain-fields. 

99. * Agropyron repens (L.) Beauv. Beginning to appear in 
gardens and fields, and threatening to become a serious 
nuisance. 

100. Elymus glaucus Buckl. Very common in dry soil, and 
extremely variable. 

101. * Triticum vulgare L. A common escape along railroads 
and in waste places. Both the bearded and beardless 
forms occur. It does not seem worth while to maintain 
Host’s T. compactum for the Western ‘‘soft’’ wheat (X). 

102. * Hordeum murinum L. Very common in waste places. 

103. * Hordeum Gussoneanum Parl. Common, especially in 
dried mud along roadsides. 

104. * Hordeum jubatum L. Only a few isolated specimens 
have been found in waste places. 

105. * Hordeum nodosum L. Common along ditches and on 
banks of streams. 

106. Sitanion jubatum J. G. Smith. Occasional on dry gravelly 
prairies about Salem (X). 

In addition to the cereals mentioned in the above list, Zea 
mays L. is a common field crop. An occasional farmer attempts 
the cultivation of ‘‘Sudan-grass” (Andropogon Sorghum (L.) 
Brot. subsp. sudanensis Piper). Miscanthus sinensis Anderss. is 
sometimes cultivated for ornament. A beautiful hardy Japanese 
bamboo of the genus Phyllostachys is a favorite among the local 
landscape-gardeners, but has never flowered. 

It will be observed that of the 106 species and varieties listed 
above, 55, or over half the entire number, are introduced, and 
51 native; and while the latter number may be regarded as fairly 
constant, the former may be expected to show a steady increase* 


* This finds further illustration in the fact that since writing the above Digitaria 
sanguinalis (L.) Scop. and Setaria glauca (L.) Beauv. have both appeared spo- 
radically in Salem. 


226 


Nothing is more striking to the casual observer than the vast 
predominance of introduced individuals in the more densely 
settled areas. Often the native species have been entirely 
crowded out, and the grass-population over large sections is 
made up exclusively of immigrants, among which the genera 
Bromus and Lolium will show the greatest number of individual . 
representatives. 

The following attempt to group our grass-species ecologically 
is far from being exhaustive, but may serve to throw a little 
more light on the general phenomena of distribution. The 

following associations may be distinguished: __ 

1. Riparian society, growing on the sand-bars and islands in 
the Willamette and Santiam Rivers, and along their muddy or 
gravelly shores, often in very dry soil: Digitaria humifusa, 
Paspalum distichum, Panicum barbipulvinatum, Aristida oligan- 
tha, Agrostis foliosa, Atra capillaris, Birger esas hypnoides, Poa 
compressa, Festuca octoflora. 

2. Hydrophyte society, growing only in water or wet ground 
along streams, borders of ponds &c.: Leersia oryzoides, Alopecurus 
aristulatus, Agrostis microphylla, A. oregonensis, Deschampsia 
caespitosa, Poa triflora, Phragmites communis, Glyceria leptosta- 
chya, G. occidentalis, G. pauciflora, G. grandis, Beckmannia 
erucaeformtis. 

3. Xerophyte society, found usually only in des soil, especially 
on the gravelly prairies: Panicum Scribnerianum, P. pacificum, 
Stipa Lemmont, Atra caryophyllea, Danthonia americana, Koeleria 
cristata, Bromus sterilis, Poa scabrella, Festuca megalura, F. 
rubra, F. idahoensis, Agropyron tenerum, Elymus glaucus, Sitanion 
jubatum. 

4. Silvicole society, generally occurring only in or at, the 
borders of open woods: Trisetum cernuum, T. canescens, Melica 
subulata, Bromus vulgaris, B. vulgaris var. eximius, Poa Howellit, 
Festuca occidentalis, F. subulata. 

5. Submontane society, restricted to the wooded lower slopes: 
of the mountains, and not extending out into the valley: Hieroch- 
loe macrophylla, Agrostis hyemalis, Pleuropogon refractus, Poa 
nervosa, P. leptocoma. 


227 


6. Ruderal society, most abundant in waste places, and often 
associated with cultivated plants: Echinochloa crus-galli, An- 
thoxanthum odoratum, Phleum pratense, Agrostis alba, Notholcus 
lanatus, Arrhenatherum elatius,. Avena fatua, A. sativa, Bromus 
carinatus, B. marginatus, B. tectorum, B. villosus, B. hordeaceus, 
B. secalinus, Dactylis glomerata, Poa annua, P. pratensis, P. 
trivialis, Festuca elatior, Lolium temulentum, L. multiflorum, 
L. perenne, Triticum vulgare, Hordeum murinum. Most of the 
others are either casual and sporadic, or occur indiscriminately 
in more than one of the above associations. 


SALEM, OREGON. 


NOTES ON COELOGYNE 
By T. D. A. COCKERELL 


Coelogyne is a remarkable genus of palaeotropical orchids, 
with over a hundred species, distributed from India to the 
New Hebrides. The type species, C. cristata Lindley, comes 
from the base of the Himalayas, and has beautiful white flowers, 
the lip marked with orange. The most remarkable thing 
about the genus is, perhaps, that the lip in some of the species is 
marked with black. I have before me a number of fresh flowers 
of C. pandurata Lindley, from Borneo. The profuse marking 
of the pale greenish lip is dull black, with a very faint rusty tint. 
The small concavity at the extreme base is cinnamon-brown. 
The other petals, and the long sepals, are pale yellowish green. 
The column or gynostemium is suffused with apple green, espe- 
cially at the tip. The bright orange pollinia rest on a broad 
crenulate or subfimbriate base. The lip is described by Nash* 
as 2-keeled, but Pfitzer and Kranzlinf treat it as 3-keeled in their 
key. There is actually a well-developed median keel, but it is 
smaller than the others. Costantint gives a colored figure of 
C. pandurata, but unfortunately it is colored bright bluish-green, 
whereas the color should be like that of Trias oblonga on the 
same plate. 


* Standard Cyclop., Horticulture. 
+ Das Pflanzenreich, 1907. 
t Atlas des Orchidées Cultivées, pl. 25, f. 1. 


228 

On examining the black markings of C. pandurata under the 
microscope and in sections, I found that they were entirely 
superficial, situated on innumerable closely placed small papillae. 
By transmitted light they appear brown, and the cinnamon 
color of the basal depression is doubtless due to the same pigment 
in dilute form. The pigment gives none of the anthocyanin 
reactions, nor does it look like anthocyanin. It is soluble in 
strong alkaline solutions, and produces a cherry-colored liquid. 
This readily stains paper, but does not change color on drying. 
Acid almost entirely discharges the brown color. J am indebted 
to Dr. F. Ramaley for the suggestion that the reactions resemble 
those of turmeric, derived from Curcuma (Zingiberaceae). The 
pigment in turmeric is curcumin, C14H;,O0;. It seems evident 
that Coelogyne possesses a closely related though doubtless 
distinct pigment. Even in species such as C. speciosa and C. 
asperata, in which the lip is marked with red or cinnamon, there 
is probably no anthocyanin at all. Pfitzer and Kranzlin remark 
that blue or blue-violet colors are lacking in the whole tribe 
Coelogynine, but the genus Pleione, to judge from the descrip- 
tions, must certainly possess anthocyanin. 

In the case of Coelogyne sparsa Reichb. f., Ames* quotes a 
collector to the effect that the flowers are white with lavender 
spots. This would suggest anthocyanin, but it must be an error, 
as others found the markings to be light brown or purplish 
brown. 


BOULDER, COLORADO 


BOOK REVIEWS 


Rock’s Lobelioideae of Hawaii T 

The flora of the Hawaiian Archipelago has long been known 
as one of the most peculiar in the world, not alone for its fan- 
tastic forms of relatives of well known plants, but for the large 
number of species that are endemic there. Its isolation is so 

-* Orchidacee, fasc 2, p. 70. 

{7 Rock, J. F. A Monographic Study of the Hawaiian Species of the Tribe 
Lobelioideae, Family Campanulaceae. Pp. I-XVI + 1-394. 217 full-page 


plates. Publication of the Bernice Pauahi Bishop Museum. Honolulu. 20 
February, 1919. 


229 
complete, the depths of the sea surrounding it so great, that there 
has been a long continuing opportunity for the fixing of types” 
and the preservation, sometimes almost unchanged from the 
earliest geological times, of ancient forms of vegetation. From 
Gaudichaud who wrote in 1826, to Wallace, Guppy, Campbell, 
and the author of the present volume, this endemic nature of 
a large part of the flora of the islands, has always been among the 
chief interests in their studies. That these few little dots in the 
limitless expanse of the Pacific should contain plants found no- 
where else in the world, and such curious plants, has almost 
dramatic significance in the general scheme of plant distribution 
in that quarter of the earth. 

Mr. Joseph H. Rock, who has studied for years the species 
and varieties of what he calls the tribe Lobelioideae of the Cam- 
panulaceae, has written a monographic quarto volume on these 
plants that clears up many points of identity which no doubt, 
have bothered some insular and continental botanists. Such 
a study, involving comparison with the types, of which there 
are photographs; delving in the literature, for which there is 
a bibliography; and settling specific and generic limits, for which, 
of course, there are keys, must be thorough to be really useful. 
Those who study the present volume can well understand that 
these features of the book have been prepared with great care 
and attention to details. Perhaps such a scholarly work will 
come as a surprise to those who have noted with not very envious 
astonishment the effects, no doubt, of the exuberant climate of 
these islands upon recent botanical production in Hawaii. 

Nearly one hundred pages are taken up with a discussion of 
the affinities of the Lobelioideae of Hawaii with those of their 
nearest relatives, which, in many cases, are geographically remote. 
The baccate genera, Clermontia, Cyanea, Delissea and Rollandia 
of American affinity, and the capsular genera Lobelia, Tremato- 
lobela and Brighamia, all woody plants except the latter, com- 
prise the tribe which is synonymous with the family Lobeliaceae, 
in the islands. These seven genera contain 149 species and 
varieties, the genus Cyanea being larger than all the others com- 
bined. It is of interest then that Mr. Rock considers this still 


230 


in process of evolution, not, like some of the other genera, 
decadent, or almost extinct as he shows for Delissea. Six of the 
Hawatian genera are endemic there, only Lobelia being found 
elsewhere. This highly endemic generic proportion naturally 
opens up many problems of distribution, ‘‘age and area’’ possi- 
bilities, and that part of the volume which discusses these 
problems is naturally the most readable. 

The reviewer recently had occasion to look over two papers on 
these islands for. Botanical Abstracts (Nos. 822 and 832, Decem- 
ber, 1918) which showed that for Hawaiian ferns and their allies 
the relationship was mostly with the east apparently because 
they are unfitted for overseas transportation; while for strand . 
plants, of which there is a high percentage of endemics the 
affinities seem to be with America. Mr. Rock shows that four 
of the Hawaiian endemic Lobelioideae, among them the numerous 
Cyaneas, are related to American genera. Not very closely 
related, however, as no Hawaiian lobeliaceous genus is actually 
in America. Lobelia, being rather generally distributed, is there- 
fore not significant in this connection. 

Of course the main portion of the book is taken up by the keys 
to species and their description and illustration. There are also 
discussions of the insect and bird visitors of the plants, flowering 
season, root systems, altitudinal range, and some account of the 
cultivated species. The book, then, is truly a monograph in 
the best sense of that much misused word.—N.T. 


FROCEEDINGS OF THE CLUB 


MEETING OF May 28, 1919 


The meeting was held in the Morphological Laboratory of the 
New York Botanical Garden, beginning at 3:30 P.M., with 
Vice-President Barnhart in the chair. There were thirteen 
persons present. 

The minutes of the meetings of April 30 and May 13 were read 
and approved. Mrs. N. L. Britton gave an informal report of 
the special meeting of the Club in conjunction with the Wild 


231 


Flower Preservation Society,.which was held at the Mansion ot 
the New York Botanical Garden on May 15 and at which Mr. 
Stewardson Brown of Philadelphia gave an illustrated lecture. 

Dr. N. L. Britton, chairman of a special committee to write a 
letter of congratulation to Capt. John Donnell Smith of Baltimore 
on the celebration of his ninetieth birthday, June 5, read a copy 
of a letter which had been drafted and this report of the committee 
was accepted by the Club. | 

Dr. F. W. Pennell, for the Field Committee, referred to the 
plans for the Memorial Day excursion, in codperation with the 
Philadelphia Botanical Club. 

Dr. M. A. Howe, for the Editorial Board, referred to a project 
for publishing the correspondence between John Torrey and 
Louis de Schweinitz and suggested authorization for its publica- 
tion in the Club’s Memoirs. On motion of Dr. N. L. Britton 
it was voted to refer the matter to the Editorial Board with 
power to publish, if the financial means could be secured. 

The resignation of Miss Amelia R. Goodlatte, Passaic, N. J., 
was accepted. 

Dr. Britton exhibited the remarkable seed-pods of a Cen- 
trolobium recently collected in Ecuador by Dr. J. N. Rose. 

The announced scientific program consisted of four communi- 
cations, as follows: 

1. ‘“Morphogenesis in Dictyostelium’’ by Dr. R. A. Harper. 
(No abstract furnished.) — 

2. Dr. Seaver showed specimens of Bulgaria globosa collected 
by Mrs. H. T. Gussow in the Liévre woods of Quebec and com- 
municated by Prof. J. H. Faull, of the University of Toronto. 
While the species has been recorded once from Ottawa, Canada, 
this is the first living specimen seen by the speaker and so far 
as he knows only the second record of the species from North 
America. The American specimens differ from the excellent 
European illustratrons by Schmidel in that the hymenium of the 
American form is much more expanded. This, however, is 
thought to be due to a difference in age and is not regarded as of 
specific importance. In all essential details the American plants 
seem to be identical with European. The speaker was especially 


232 


glad to receive specimens of this plant since a monograph of this 
group for North America is in process of preparation. 
“Canadian Arctic. Mosses,” by Mr. R. S. Williams. 

A list made by the speaker enumerates 68 species of mosses 
collected by various members of the expedition sent out by the 
Canadian Government, in connection with the Geological Survey 
of Canada, to the northern coasts of Alaska and British North 
America in 1913~’16. The genus most largely represented is 
Drepanocladus with 11 species, all sterile; next comes Bryum 
with 9 species, 5 of which are fruiting; all the other genera, 33 
in number, are represented by I or 2 species except Dicranum, 
of which there are 3, one of which, D. elongatum, is in fruit. 

The greatest number of species (7) separated out from one 
collection and growing more or less intimately associated , occurs 
under no. 60, representing a piece of sod, some 4 by 6 inches on 
the upper surface, cut out from the tundra on Barter Island, on 
the coast of Arctic Alaska. The species, all sterile and men- 
tioned in the order of their abundance, the commonest first, 
are as follows: Catoscepium nigritum, Swartzia montana, Dre- 
panocladus brevifolius, Bryum neodamense, Chrysohypnum stel- 
latum, Encalypta brevicolla, and Drepanocladus scorpioides. 
Under no. 23, a small collection made 50 miles inland from Cam- 
den Harbor, Alaska, the following were separated out: Bryum 
pallescens, Leptobryum pyriforme, Mnium affine, Drepanocladus 
aduncus, and Rhytidium rugosum, the Bryum and Leptobryum 
bearing fruit. The specimens are sterile unless otherwise stated. 
One species, Bryum nzodamense, found in Europe, from the 
Pyrenees to the Arctic coast, does not seem to have been credited 
before to America. Anothér, Drepanocladus brevifolius, has 
been noted from Greenland only, while two others are described 
as new. The region collected over extends from about 68° to 
70° 35’ N. and from the northern Alaska coast eastward to about 
long. 110° W. 

4. “Types of Sterility in the Radish,” by Dr. A. B. Stout. 

Dr. Stout exhibited living plants of cultivated races of the 
radish, illustrating three types of sterility as follows: (1) blasting 
of flowers, (2) self- and cross-incompatibility, (3) embryo abor- 


233 


tion after fertilization. A brief report was made of the progress 
and results of experimental studies on these types of sterility 
in this species. 

After the presentation of the papers, they were discussed 
briefly by some of the members present. 

Adjournment followed. 

MARSHALL A. Howe, 
Secretary pro tem. 


| 
Dis 
wea 
wal » 


The Torrey Botanica] Club 


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Committees for 1919. 


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R. A. HARPER, Chairman, Mrs. E. G. BRITTON, Chairman. 
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Field Committee Phanerogams: Cryptogams: 
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Mrs, L. M. KEELER N. L. BRITTON T. E. Hazen 
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F. J. SEAVER 


Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M. 
Liverworts: A. W. Evans ; Richards 
Fresh Water Algae: T. E. Hazen 7 Hypocreaceae,- Perisporieae, Plectas- 
Marine Algae: M. A. Howe cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C. Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M.. Richards, F. 
Except Russulaand Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 

Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 

Polyporeae: M. Levine Chytridiaceae, 
Exobasidii: H. M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive Yeast and Bacteria: Prof. J. Broadhiss 


Discomycetes: B. O. Dodge Insect galls: Mel T. Cook 


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Vol. 19 December, IgIg No. 12 


TORREYA 


A MonruHiy JournaL or Boranicat Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873. 


CONTENTS 

‘Scrophulariaceae of the local Flora. FRANCIS W. PENNELL: . . ee S235 
The Occurrence and Distribution of psig’ s Pondweed in Northeastern Ohio. 

By Ao SELOPKING sy Soe Bie he a ehis eas UREN, rea BC NEI NP Se ae nile 243 
Shorter Notes 

Carpolites macrophyllus a Philadelphus. T.D. A, CockEREIL. ....., 244 
Reviews 

Flora of the District of Columbia. N.L. Britton. . 2... . tee Ne  2h4 
Peneeefanis of the Chub 2.21 od aye Ae 2 ie ea eh RE pg 
News Items baa x3 “dar 0) | aro Me BR Te AD 4, _. 248 
‘ Dates of Publication -....:; ... echo nee Sexclet 3 “ sO agg 
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PUBLISHED FoR THE CLUB 


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TORREYA 


Vol. Ig No. 12 
December, IgIg 


SCROPHULARIACEAE OF THE LOCAL FLORA. V 


By Francis W. PENNELL 


Concluded from November TORREYA 


16. BUCHNERA L. Sp. Pl. 630. 1753 
Type species, B. americana L. 


I. BUCHNERA AMERICANA L. l.c. 630. 1753. ‘‘Habitat in 
Virginia, Canada.” Based upon Gron., Fl. Virg. 74. 
1743, typified by Clayton 142 from Virginia. Type not 
verified, but description distinctive. 

Flowering in July, fruiting in August and September. 

Sandy or sterile loam soil, occasional in the Piedmont Region 
in the southwestern extremity of our area. Delaware County, 
Pennsylvania (Williamson School), Lancaster Co. (Pleasant 
Grove), and in Newcastle Co., Delaware (Centreville). Ranges 
from Pennsylvania to Florida, southern Ontario, Illinois and 


Louisiana. 
17. SCHWALBEA L. Sp. PI. 606. 1753 
Type species, S. americana L. 
I. SCHWALBEA AMERICANA L. l.c. 606. 1753. ‘‘Habitat in 


7 


America septentrionali.’”’ Linné had in his herbarium no 

specimen of this, so that his species is based wholly upon 

Gron., Fl. Virg. 71. 1743, typified by Clayton 33 from 

from Virginia. This from the description of the leaves 

as lanceolate and the plant as quite pubescent would 
appear to have been the species now considered. 

Flowering from mid-June to early July, fruiting in September. 

Sandy soil, usually rather damp, in pineland and about edges 

of salt-marsh, in the Coastal Plain of southern New Jersey and 


[No. 11, Vol. 19, of TORREYA, comprising pp. 205-233, was issued 18 Dec., 1919.] 
e 


235 


236 


in central Delaware. Ranges from southeastern Massachusetts 
to Virginia, so is to be expected in eastern Long Island. 


18. CastTiLLEyJA Mutis; L. f. Suppl. 293. 1781 
Type species, C. fissifolia L. f., of Colombia 
I. CASTILLEJA COCCINEA (L.) Spreng. 
Bartsia coccinea L. Sp. Pl. 602. 1753. ‘Habitat in Vir- 
ginia, .Noveboraco . . . Hort. Cliff. 235.” From Ey 
Hort. Cliff. 325. 1737, °Crescit in Virginia, unde 
delatam communicavit DD. Gronovius,’’ and from 
Gron., Fl. Virg. 69. 1743, Clayi.n. 293.”  Clayionzaz: 
the type, must be certainly the species here considered. 
Rhinanthus coccineus (L.) Lam. Encyc. 2: 60. 1786. 
Euchroma coccinea (L.) Nutt. Gen. N. Am. Pl. 2:55. 1818. 
Type of the genus Euchroma Nutt. 
Castilleja coccinea (L.) Spreng. Syst. 2: 775. 1825. 

Flowering from late April to early June, an soon ripening 
fruit. 

Meadows and moist grassy slopes, loam or sandy loam, through 
the Piedmont Region, more frequent westward; in the Coastal 
Plain occasional in the Middle District of southern New Jersey. 
Ranges from Maine to Manitoba south ‘to South Carolina and 
Kansas. 

19. RHINANTHUS L. Sp. Pl. 603. 1753 
Type species, R. Crista-galli L., of Europe 
1. RHINANTHUS CRISTA-GALLI L. 

Flowering in May and early June, fruiting in late June. 

Fields and open places near Stratford, Connecticut. Probably 
introduced from Eurasia, although said to be native north- 
eastward. 

20) -EEDICULARIS L.) Sp. Pl-607. 2ryse 
Type species, P. palustris L., of Europe 


Stem 6-8 dm. tall, glabrous. Leaves shallowly lobed, the 
sinuses narrow, the lobes with minute regular crenations. 
Bracts auriculate near base. Rachis of inflorescence glab- 
rous. Fused sepals of each side terminating in a slightly 
enlarged crenate foliar tip, glabrous or with a very few long 
hairs near base. Corolla with truncate apex of posterior 


lobes without tooth-like processes. Capsule brown, scarcely 
exceeding calyx, slenderly beaked. Flowering in late 


summer. 1. P. lanceolata. 
Stem 1-3 dm. tall, hirsute, especially above. Leaves deeply 

lobed, the sinuses broad, the lobes with more prominent 

irregular crenations. Bracts entire near base. Rachis of 

inflorescence lanate. Fused sepals of each side broadly 

acute, entire, pubescent along the veins. Corolla with apex 

of posterior lobes each with a tooth-like process. Capsule 

straw-colored, twice as long as the calyx, scarcely beaked. 

Flowering in spring. 2. P. canadensis. 
I. PEDICULARIS LANCEOLATA Michx. Fl. Bor. Am. 2:18. 1803. 

“Hab. in regione Illinoensi [A. Michaux].’’ Type not 
verified, but description distinctive. 

Pedicularis auriculata Sm. in Rees Cycl. 26: 1813. ‘‘Sent 
by the Rey. Dr. Muhlenberg, from the neighborhood of 
Lancaster in Pennsylvania.’”’ Description distinctive. 

Pedicularis pallida Banks; Pursh, Fl. Am. Sept. 424. 1814. 
“In a swamp near Kings-bridge, New York. . . . Ph. [= 
Pursh| . . . v.v.; v.s. in Herb. Banks.”’ Description dis- 
tinctive. 

Flowering from late August to late September, fruiting late 

September and October. 

Swales and moist meadows, loam soil, in the Piedmont region, 
more frequent southwestward; occasional in the Middle District 
of the Coastal Plain of southern New Jersey, extending nearly 
to Cape May. Ranges from Massachusetts to Manitoba, 


North Carolina and Nebraska. 


2. PEDICULARIS CANADENSIS L. Mant. 86. 1767. ‘‘Habitat in 
America septentrionali. Kalm.” Description distinctive. 
Pedicularis gladiata Michx. Fl.’ Bor. Amer. 2: 18. 1803. 
“Hab. in Pennsylvania [A. Michaux]. Description 
quite distinctive. 

Flowering from late April to late May, fruiting in late May and 

early June. | 
Woodland, or on knolls in meadows, loam or sandy loam, 
common throughout above the Fall-Line; in the Coastal Plain 
frequent or occasional in Long Island and in the Middle District 
of southern New Jersey. Ranges from Nova Scotia to Manitoba, 

* south to Florida and Texas. 


258 


21. MELAMPYRUM L., Sp. Pl. 605. 1753 
Type species, M. cristatum L. of Europe 


Main stem-leaves linear or lanceolate-linear. Bracts 

conspicuously fimbriate near base, with teeth fre- 

quently as long as the width of the blade. Capsules 

mostly 6-7 mm. long, curved and usually attenuate- 

beaked. Seeds 2-2.5 mm. long, brown to blackish. 1. M. lineare. 

Main stem-leaves linear-lanceolate to nearly ovate. 

Bracts slightly or not fimbriate near base, the teeth 

shorter than the width of the blade. Capsules fre- 

quently larger, reaching 8-9 mm. long, slightly or 

not curved and less or not attenuate-beaked. Seeds 

often larger, reaching 3 mm. long, usually black. ta. M. lineare latifolium,. 
1. MELAMPYRUM LINEARE Desr.; Lam. Encyc. 4: 22. 1796. 

‘“‘Rapportée de la Caroline par M. Fraser... (w.s.)” 
Description made from a very small and young plant, 
but certainly of the form here considered. Characteriza- 
tion of calyx as 5-toothed surely erroneous. 
Flowering from mid-June to September, and soon ripening 
fruit. 

Sandy soil, pineland and in open deciduous woodland, common 
throughout the Coastal Plain; inland occasional and mostly 
transitional to var. latifolium. Ranges from Massachusetts to 
North Carolina, and, including varieties, inland northward 
across the continent. 


Ia. MELAMPYRUM LINEARE LATIFOLIUM (Muhl.) Beauverd 

Melampyrum americanum Michx. Fl. Bor. Amer. 2: 16. 
1803. ‘‘Hab. a sinu Hudsonis ad montosam Carolinam. 
[A. Michaux:.”’ Description evidently of the prevalent 
inland broader-leaved plant. 

Melampyrum latifolium Muhl. [Cat. 57. 1813. nomen 
nudum]; Eaton, Man. Bot. N.& M. St. ed. 11 316. 1818. 
From Muhlenberg’s Catalog, the type station is in Dela- 
ware. Type not seen, but evidently is of the inland 
broader-leaved plant. 

Melampyrum americanum latifoliwum (Muhl.) Eaton, l.c. ed. 
LL. 350.7 S22. 

Melampyrum pratense americanum (Michx.) Benth. in DC. 
Prod. 10: 584. 1846. 


239 


Melampyrum lineare latifolium (Muhl.) Beauverd in Mem, 
Soc. Phys. Genéve 38: 474. 1916. 

Melampyrum lineare americanum (Michx.) Beauverd, l.c. 
476. 1916. Beauverd distinguishes latifoliwm with bracts 
broader, the lower entire, the upper entire or few-toothed, 
and the first flower placed at the third or fourth node, 
from americanum with bracts narrower, the lower entire 
or slightly toothed, the upper always toothed, and the 
first flower in the axil of the fourth to eighth node. His 
americanum is transitional from Jatifolium to lineare 
itself, from which he distinguishes both these varieties as 
having corolla whitish, tinged with purple, instead of 
pale-yellow, tinged with purple. The corolla of the 
species, as well of var. /atifolium as I understand it, has the 
corolla white, posteriorly more or less tinged with red, 
especially in age, and only the palate yellow. His color 
distinction cannot be maintained, and I should consider 
the broadest, most entire-leaved plants as an extreme of 
this variety. 

Flowering from late May to mid-August, and soon ripening 
fruit. 

Dry open woods, in potassic soil, sandy or sterile, locally 
common on sandstone or shale ridges, etc., throughout the area 
above the Fall-line; in the Coastal Plain occasional on Long 
Island and in the Middle District of southern New Jersey. 
Intergrading to the species. 


LocaL SPECIMENS OF THE AUTHOR’S COLLECTING 


As my own collections illustrating our local species of Scro- 
phulariaceae in part have already been, and in part are soon to 
be, distributed to various herbaria, it may be well here to present 
a summary of the numbers of these. The specimen numbers 
will be grouped by species and states. All are from the local 
flora as defined in the introduction to these studies. 

Agalinis acuta (N. Y.) 5292, 6551, 6552, 9340, 10126. 
Agalinis Holmiana (N. Y.) 10167. (N. J.) 1662, 2695, 3544, 
3583, 3628, 6483, 9117. 


240 


Agalinis maritima (N. Y.) 9359. (N. J.) 1807, 2157. 

Agalinis purpurea (N. Y.) 5291, 6549, 6647, 9366, 10146. (N.J.) 
2602, 2603, 2604, 4004, 6492, 6524, 6637, 9294. (Pa.) 
476, 750, 786, 838, 847, 1660, 2682, 2689, 3598, 3609, 5182, 
5272, 8984. 

Agalinis tenuifolia (Conn.) 8578. (N. Y.) 6651, 6698, 9226. 
(N. J.) 1664, 6534, 9870. (Pa.) 658, 837, 1642, 2681, 2688, 
2690, 3543, 5289, 8906. 

Agalinis virgata (N. J.) 2692, 2694, 3584, 3626, 3808, 6521, 
6523, 9114. 

Aureolaria flava (N. Y.) 5293, 8434, 9407. (N. J.) 8358. (Pa.) 
3541, 3624, 5225, 5260, 5284, 5286, 6791. 

Aureolaria pedicularia (N. Y.) 9225, to171. (N. J.) 10040. 
(Pa.) 583, 991, 1948, 3542, 3559, 3585, 3589, 3625, 5192, 
5226, 5201,. 5262, 5265, 5288, 8831, 8860: | (Delljegue 
(Md.) 1619. 

Aureolaria pedicularia caesariensis (N. J.) 1837, 3545, 3627, 
6487, 9155. 

Aureolaria pedicularia intercedens (Pa.) 676, 4982. 

Aureolaria virginica (N. Y.) 5294, 6868, 8459. (N. J.) 3546, 
3986, 6489, 7363, 7428, 8345, 9208. (Pa.) 337, 4985, 5021, 
5067, 5227, 5259, 5283, 6503, 6793, 7850, 7912, 8847, 9412. 
(Del.) 7754. (Md.) 1615. 

Castilleja coccinea (Pa.) 1290, 2034, 2772. 

Chelone glabra (N. Y.) 6643, 6678, 6745, 6833, 6898, 8604, 9239, 
9308, 9397, 9400. (N. J.) 6485, 6525, 6543, 9223, 9224. 
(Pa.) 6794. | 

Chelone glabra f. tomentosa (Pa.) 901, 6480, 8827, 8861, 8912. 

Gratiola aurea (N. J.) 6500, 6527, 9929. 

Gratiola aurea obtusa (N. J.) 9897. 

Gratiola neglecta (Conn.) 8579. (N. Y.) 9930. (N. J.) 7367, 
9445. (Pa.) 1495, 2822, 5013, 6477, 6994, 7256, 7861. 

Gratiola pilosa (N. J.) 6486, 6401. 

Gratiola virginiana (N. J.) 6495. 

Hemianthus micranthus (N. J.) 6497. 

Ilysanthes dubia (N. Y.) 6704 p.p., 8429. (N.J.) 6493. (Pa.) 
6467, 6474 p.p., 8014, 8837. 


241 


Ilysanthes dubia inundata (N. J.) 6496. : 

Ilysanthes inaequalis (N. Y.) 6704 p.p. (N. J.) 3987, 6494, 
6636. (Pa.) 6474 p.p. 

Limosella subulata (N. J.) 6635. 

Ltmaria canadensis (N. Y.) 7747, 10143. (N. J.) 6488, 6520, 
6971, 6972, 8182, 9438, 10012, 10021, 10077. (Md.) 8882. 
Linaria Linaria (N. Y.) 6699, 7014, 7679, 8710. (N. J.) 6526, 

6548, 7408. (Pa.) 7303, 7968. (Md.) 8881. 

Melampyrum lineare (N. J.) 3572, 3818, 3836, 6499, 6522, 6587, 
8167, 9050. (Pa.) 1883, 6481. 

Melampyrum lineare latifolium (N. Y.) 6795, 6798, 8440. (N. J.) 
7429, 9219, 9460, 10010, 10054, 10118. (Pa.) 1561, 6501, 
6795, 7880, 7956, 8852. 

Mimulus alatus (N. Y.) 7683, 82009. 

Mimulus ringens (N. Y.) 6550, 6642, 6683, 7636, 8687, 9190, 
9305. (N. J.) 6537. (Pa.) 6472, 6476, 6502, 7857, 7889, 
8028, 8842, 8958. 

Otophylla auriculata (Pa.) 5229, 5230, 5285, 5290. 

Pedicularis canadensis (N. Y.) 2386, 6761, 6823, 6905, 7153, 
8433, 9951, 9968, 10141. (N. J.) 6974, 9995. (Pa.) 2612, 
6792, 8753. 

Pedicularis lanceolata (Pa.) 1839, 6469. 

Penstemon Digitalis (N. Y.) 9423. (Pa.) 6471. 

Penstemon hirsutus (N. J.) 7409. (Pa.) 3645, 6716, 7006. 

Penstemon pallidus (N. Y.) 7130. 

chwalbea americana (N. J.) 9028, 10086. 

Scrophularia leporella (N. Y.) 6790, 6888, 6910, 7732, 8323. 
(N.J.) 10098. (Pa.) 4993. 

Scrophularia marilandica (N. Y.) 8220. (N. J.) 9904. (Pa.) 

6468, 6504, 8108. 

Verbascum Blattaria (N. J.) 7053. (Pa.) 6475, 7971. 

Verbascum Lychnitis (Pa.) 6478. 

Verbascum Thapsus (N. Y.) 6684, 8324, 8496. (Pa.) 6479, 7970. 

Veronica americana (N. Y.) 6824, 6887, 7186, 7740. (N. J.) 
6533, 9437. (Pa.) 5069, 7238. 7 

Veronica ,arvensis (N. Y.) 6787, 6867. (N. J.) 7062, 9993. 
(Pa.) 6719, 6999, 7254. 


242 


Veronica Brittonit (N. J.) 10100. 

Veronica Chamaedrys (N. Y.) 6768. 

Veronica officinalis (N. Y.) 6880, 7023, 7118, 7623, 8423. (N. J.) 
6528, 7414. (Pa.) 6718, 7965. 

Veronica peregrina (Pa.) 6995. 

Veronica scutellata (N. Y.) 6641. 

Veronica serpyllifolia (N. Y.) 6788, 6830, 6911. 

Veronica Tournefortii (Pa.) 6466. 

Veronicastrum virginicum (N. Y.) 7731, 8697, 9851. (N. J.) 
6529, 10104. (Pa.) 373, 4980, 4981, 6470, 7778, 8003, 8082, 
9000, 9016. 

ADDITIONS AND CORRECTIONS 


Page 111, line 19.—Delete word “persistent.” The tubercle- 
like base of the style lasts but a short time after anthesis, not 
until the fruit is mature. 

Page 111, last line —VI. VERONICEAE, not ‘“ DIGITALEAE.” 

Page 112, line 9 —Add word “‘usually”’ before “parasitic.”’ 

Page 112, line 19.—Add word “‘one”’ so as to read “Two stig- 
matic lines, one down each side of style-apex.”’ 

Page 112, line 22.—Add to characterization of genera contrasted 
with Buchnera, ‘‘ Calyx not bracted at base.” 

Page 113, line 12.—Add to characterization of Buchnera, “ Calyx 
bibracteolate at base.” 

Page 113, line 19.—Add to characterization of Schwalbea: 
“Calyx bibracteolate at base.” © 

Page 113, line 22.—Add to characterization of genera contrasted 
with Schwalbea, ‘‘Calyx not bracted at base.” 

Page 114, line 10.—Add phrase ‘‘to four’’ so expression reads 
‘“‘Seeds maturing two to four to a capsule.” 

Page 152, line 13.—Add ‘“‘ Linaria canadensis occurs occasionally 
in a pink-flowered form.”’ 

Page 168.—13. Veronica Brittoni Porter and Page 170.—14. 
Veronica glandifera Pennell.: It should have been stated that 
both these newly described species are segregates from the 
complex. known as Veronica Anagallis-aquatica L. This 
name belongs to some one of several Palaeartic species, all 
of which differ from our plants. 


243 


THE OCCURRENCE AND DISTRIBUTION OF VASEY'S 
PONDWEED IN NORTHEASTERN OHIO 


By L. S. HopkKINS 


So far as available records show the first collection of this 
interesting little pondweed—Potamogeton Vaseyi Robbins— 
was made at Brady’s Lake, Portage Co., by the writer on June 
22, 1912, it being in flower at the time. 

The fact that the plant was new to me at the time of its col- 
lection signified little since I had given no attention to the mem- 
bers of this genus. Moreover it occurred in such abundance 
that I never surmised that it had not been collected before and 
it was not until later that I learned that this was the first authen- 
tic account of its occurrence in the state. 

It has since been collected by Mr. John Bright of Glenshaw, 
Pa. at the mouth of Cowles Creek, near Geneva-on-the-Lake in 
Ashtabula Co. on July 28, 1918, and by myself in August, 1918, 
and again in 1919 at Sandy Lake (also called Lake Stafford), 
Portage Co. 

Although the Gray’s New Manual, 1908, page 76, gives its 
distribution as being from ~ Me: fO-Oiite 3S: tO be NER a) 
Ill., and Minn.,’”’ Schaffner does not include it in his ‘‘Ohio 
Catalogue of Vascular Plants.” 

Brief comment may be made upon two statements commonly 
made in connection with this plant. The first is found in Britton 
and Brown’s Illustrated Flora, 1913, page 83 to the effect that 
‘“‘emersed fertile forms (occur) in shallow water.’’ The other is 
found in the Gray’s New Manual, which states that the ‘fruiting 
form with floating leaves (is)rare.”’ 

With reference to local material as studied at the lakes men- 
tioned, it seems worthy of note that it does not agree with the 
manuals quoted in three essential particulars. 

1. Fruiting stems are not rare. On the contrary they are very 
abundant. It is no exaggeration to say that enough fruiting 
stems to fill an ordinary row boat could have been collected at 
Sandy Lake in August, 1919. 


244 


2. Unless the term “floating leaves”’ is used merely to distin- 
guish the larger leaves from the smaller it is a misnomer, for 
they do not always float. Thousands of these “floating leaves” 
were seen in 1918 and again in 1919, which by actual measure- 
ment, were submerged at varying depths up to twenty inches. 

3. Fruiting stems are not limited to shallow water. It pro- 
duced fruit abundantly at Sandy Lake in 1919 in water of such 
depth that the combined length of an ordinary oar—6 ft, 6 in.— 
and my arm with the sleeve rolled up as far as I could get it did ~ 
not suffice to reach the bottom. In this particular lake for the 
past two seasons it has fruited most abundantly in water over 
Sixsicetiacep: 

As northeastern Ohio abounds in small lakes it is not improb- 
able that other stations for it will be discovered. 

Several sheets of herbarium material were prepared from 
specimens collected at Sandy Lake and will be given to any one 
who may care to send postage for it. 


STATE NORMAL COLLEGE, 
KENT, OHIO. 


SHORTER NOTES 


Carpolithes macrophyllus a Philadelphus.—In ToRREYA, I911, 
p. 235, I described a fossil fruit from the Miocene of Florissant, 
giving it the name Carpolithes macrophyllus, and leaving its 
classification uncertain. I now find that it agrees in every 
particular with Philadelphus, except that the sepals are longer 
than in any living species known to me. It must be called 
Philadelphus macrophyllus, but it very likely belongs to the 
same species as P. palaeophilus Ckll. 1908, based on leaves from 
the same rocks.—T. D. A: COCKERELL 


REVIEWS 
Flora of the District of Columbia* 
Washington botanists are to be congratulated upon the 
publication of this important contribution to the regional botany 
of eastern North America, containing, as it does, the record of an 


* Hitchcock, A. S. and Standley, P. C.* With the assistance of the botanists of 
Washington, Flora of the District of Columbia and Vicinity. Contribution U. S. 
Nat. Herb. 21: pp. 1-329, pl. 42. I9I9. 


245 


immense amount of original observation by many students over 
many years. There is a brief introduction, describing the geo- 
graphic, geologic, and ecologic aspects of the area, which is in a 
general way a circle of fifteen miles radius with the Capitol as 
the center and which has yielded 1,630 species of native and 
naturalized plants here formally listed, with records of habitat, 
distribution, and common names. Numerous other species, found 
adventive or as waifs are mentioned in notes and there are 
occasional critical comments on relationship, morphology, uses 
and other features. 

The Catalogue is preceded by a key to the families based 
mainly on vegetative characters and by another key to the 
families based mainly on floral characters, these two keys occu- 
pying 30 pages of the book, and they have been very ingeniously 
worked up; there is a generic key for each family and a species 
key for each genus. The families have not been grouped in 
orders, which is to be regretted. Asa rule, the keys are detailed 
and complete enough to effect the determination of species, 
assuming a general knowledge of the flora by the student using 
the work. Varieties or races are very sparingly admitted and 
the recognition of species is commendably sane. Thus only 
seven species of Crataegus are listed, only 6 Rubi, only 3 Lacin- 
arias, and only 6 Antennarias, with an apology for one of them. 
Oenothera biennis is very properly disposed of as ‘‘an extremely 
variable species . . . considered to consist of numerous ‘ele- 
mentary species.’’’ Generic ranks are for the most part liberally 
recognized, perhaps not in all families consistently, this doubtless 
referable to the very considerable number of collaborators 
(twenty-two). It would be most unfortunate to have any- 
thing like that number of students of the same turn of mind; 
thus Padus is not separated from Prunus, while Persicaria is 
kept out of Polygonum. 

A few generic names replace those in ordinary usage, as 
Bilderdykia for Tiniaria and Campe for Barbarea, having priority 
of publication. Several specific names are likewise strangers, 
due to bibliographic research and the more correct application 
of names to type-specimens, noteworthy those ferreted out by 


246 


Dr. Blake in his studies of Linnaean species while in London a 
few years ago. One of these I have supposed might be based 
on some ancient error or mixture; that is the application of the 
name Eleocharis capitata to what we have long been calling 
Eleocharis tenuis; it seems incredible that Linnaeus could have 
meant to describe the spikelet of that sedge as subglobose and 
to have assigned the name capifata to it. Linnaeus reached 
some results which seem queer to us, like his classifying Lysz- 
machia terrestris as a Mistletoe and Comptonia peregrina as a 
Liguidambar, but these flukes are brilliant as compared with ~ 
calling the spikelet of Eleocharis tenuis subglobose. 

It goes without saying that the nomenclature of the District 
Flora follows the American Code, rather than the so-called 
International Code forced down the throats of the Vienna 
Botanical Congress by a German majority and further manipu- 
lated by the same majority at the Brussels Congress; we can 
well understand why the French have never recognized it as 
valid, and why anybody but Germans or Austrians should so 
regard it has always been a puzzle, especially as the American 
Code is much more logical and cuts out autocracy. Internation- 
alism is proving a dangerous principle to play with, and in many 
aspects has much to condemn it. 

The Washington botanists have followed the American Code 
consistently in almost every item except the use of duplicate 
binomials; they do not say why these have not been used; 
zodlogists have used them for many years without losing sleep, 
and Sassafras Sassafras runs well with Corvus Corvus. We must, 
I suppose, conclude that our colleagues of the fifteen-mile 
circle around the national Capitol, or most of them, simply do 
not like to say Catalpa Catalpa, although by refusing such 
diction they lose the valuable suggestion that Linnaeus named 
the tree Bignonia Catalpa. Or may it be that they are influenced 
by the line of thought advanced by Engler at the Vienna Con- 
gress when we asked him why he objected and he told us prin- 
cipally that such names had made some of his students laugh! 
And so the risibility of juvenile Huns prevented their adoption 
at that highly amusing convocation. 

N. L. BritTTON. 


247 


PROCEEDINGS OF THE CLUB 
OCTOBER 14, I919 

The meeting was held in the lecture room of the Department of 
Botany, Columbia University, President Richards presiding. 
There were seventeen persons present. 

The minutes of May 28 were read and approved. 

The following persons were nominated and elected to mem-- 
bership: Mr. Hilary S. Jurica, St. Procopius College, Lysle, 
Illinois; Mr. Frederick Kobbé, 103 East 86th St., New York City; 
Miss Ella McNeier, 260 Convent Ave., New York City; Mr. 
Charles Brown, 762 Courtlandt Ave., New York City; Mrs. 
D. W. Johnston, 206 East 200th St., New York City; Miss 
Nessa Cohen, 2094 Fifth Ave., New York City; Miss Marguerite 
Gluck, 2010 Seventh Ave., New York City. 

Dr. Seaver called for suggestions regarding the programs for 
the evening meetings of the Club. 

The announced program called for reports by members on 
their summer work. 

Professor R. A. Harper exhibited a number of very excellent 
photographs of species of Boleti collected at various times during 
the summer in the vicinity of Woods Hole, Mass. 

Dr. M. A. Howe gave a brief account of the life of C. C. Frost 
mentioned by Dr. Harper. He also spoke of his own work in 
connection with the establishment of the dahlia border at the 
New York Botanical Garden. He has obtained for the garden 
some 343 varieties of dahlias. 

Dr. H. B. Douglas remarked on the various species of Boleti 
he had collected in Maine. 

Professor T. E. Hazen spoke of his work on the Pontederias 
at Woods Hole. He had gathered nineteen plants from the 
field and transplanted them successfully in a small pond where 
they could be studied and photographed conveniently.: He 
showed a numberof pictures, using his negatives as lantern 
slides as his pictures had not been finished. 

Mr. A. T. Beals spoke of collecting mosses during the summer. 
His material has not been worked over as yet but contains many 
interesting species. 


248 


B. O. Dodge exhibited a few photographs of Gymnosporangium, 
Sporodinia and Exobasidium which had been taken at Woods 
Hole by Professor Harper, Professor Hazen, and himself. 

Professor Richards exhibited several beautiful specimens of 
Buellia geographica which he and Mrs. Richards had collected 
at Glacier Park, Montana, during the summer. The gas analyses 
which he had been making during the summer have not been 
completed sufficiently to warrant reporting at this time. He also 
exhibited a large specimen of Calvatia gigantea collected recently 
in this vicinity. 

Adjournment followed. 

B. O. DonGE, Secrétary. 


NEWS ITEMS 
At the St. Louis meeting of the Ecological Society of America 
The Plant World was taken over by the Society and will be 
merged with Ecology, a new journal which will be issued as the 
official organ of the Society. 


Beginning with volume 20 TorREyA will be issued bi-monthly. 
This has been decided because of the greatly increased cost of 
production. As heretofore its pages will be open to all who have 
something to say of interest to botany, but if more material is 
offered for publication than we have room for, preference will be 
given to members of the Club, and to notes on local botany. 


249 


. DATES OF PUBLICATION 
Pages 1-20 Issued February 


1, for January 


2; 
3) 


February 
March 
April 

May 

June 

July 
August 
September 
October 
November 
December 


21-36 
37-56 
57-84 
85-105 
107-124 
125-142 
143-160 
161-185 
187-204 
205-234 
235-257 


March 
May 

June 

July 
August 
September 
September 
October 
December 
December 
January 


28, 


1919 
1919 
1919 
1919 
1919 
1919 
1919 
1919 
1919 
1919 
1919 
1920 


> 


INDEX TO VOLUME NINETEEN 


[The names of species and varieties described as new and of new combinations 


are in bold face type.] 


Aaronsohn, A., death of, 203 


Abrams, L. R., A New California 
Cypress. Cupressus nevadensis sp. 
nov.,)- 


Abstracts and Criticisms of Botanical 
Papers read at the Baltimore Meeting 
of thevAv vA, A Ss) 83) 

Acer circinatum fulva, 182; floridanum, 
121 ¥ 

Achillea millefolium, 12 

Adams, C. C., 84, 159 

Agalinis, 112; acuta, 210, 214, 239; 
decemloba, 210, 314; Holmiana, 210, 
213, 230; maritima, 200, 210, 2IT, 
240; palustris, 209, 212; paupercula, 
210, 211; purpurea, 210, 212, 240; 
tenuifolia, 210, 214, 240; virgata, 
210, 213, 240 

Agoseris villosum, 182 

Agropyron brevifolium, 193; caesium, 
189; dasystachyum, 193; divergens, 
193; Elmeri, 193; glaucum, 189; 
junceum, 189; pungens, 189; repens, 
225; tenerum, 225, 226 

Agrostis alba, 188, 220, 227; aspetifolia, 
190; attenuata, 191; densiflora, I91; 
foliosa, 220, 226; geminata, I091; 
grandis, 191; Hallii, 220; hyemalis, 
220, 226; micropetala, 220; micro- 
phylla, 226; oregonensis, 220, 226; 
pallens, 188; Pringlei, 191; scabra, 
I91; Scouleri, 191; tenuiculmis, 191; 
varians, I91; verticellata, 191; vires- 
cens, I9QI 

Aira capillaris, 189, 221, 226; caryo- 
phyllea, 221, 226; praecox, 221 

Alopecurus aristulatus, 220, 226; geni- 
culatus, 191; pallescens, 191; praten- 
sis 220 

American Museum of Natural History, 
meetings at, 18, 34, 102, 104, 123, 
158 

Ammophila arenaria, 188 

Andrews, A. L., Bryological notes— 
V. Scapania nimbosa from Norway, 
49 

Andrews, E. F., The Japanese Honey- 
suckle in the Eastern United States, 
37 

Andromeda, 153 


bo 


Andropogon Sorghum, 225 
Androsace, 180 
Anemone patens, 182 
Anogra, 175 
Anthoxanthum odoratum, 
Puelii, 188, 219 
Antirrhinum canadense, I51 
Apera spica-venti, 188, 220 
Aplectrum, 155 
Aquilegia caerulea, 137-141; caerulea 
x chrysantha, 139; caerulea daileyae, 
I37; caerulea x desertorum, 139; 
chrysantha, 138; desertcrum, 138; 
desertorum x chrysantha, 139; ele- 
gantula, 138; vulgaris stellata, 137 
Arabis, 181 
Arethusa, 153 
Argentina, 175 
Aristida fasciculata, 
220, 226 
Arnica alpina, 18 
Arrhenatherum elatius, 221, 227 
Arthur, J. C., A Correction, 83; New 
Names for Species of Phanerogams, 48 
Aster cordifolius, 12; divaricatus, 12; 
dumosus, 12; ericoides, 12; lateri- 
florus, 12; novae-angliae, 12; pani- 
culatus, 12; patens, 12; Tradescanti, 
12; undulatus, 12; vimineus, 12 
Astrasalus, 181 
Athysanus pusillus, 184 
Aureolaria, 112; flava, 206, 208, 240; 
glauca, 209; laevigata, 206, 208; 
pedicularia, 205, 206, 240; pedi- 
cularia ambigens, 207; pedicularia 
caesariensis, 205, 207, 240; pedi- 
cularia intercedens, 205, 207, 240; 
villosa, 205, 207; virginica, 49, 205, 


BMG), 22%7)> 


t90; oligantha, 


207, 240 

Avena barbata, 189, 221; fatua, 191, 
221, 226; fatua glabrata, 221; sativa, 
221, 227; Smithii, 191 


‘Bailey, L. H., 142 

Baptisia tinctoria, 12 

Barnhart; J. His 27; 10; 38 1Oouoas 
157, 230 

Bartsia coccinea, 236 

Batrachium, 175 

Beals, A. T., 247 


251 


Berry, E. W., 19, 203; Pleistocene 
Plants from. Tennessee and Missis- 
sippi, 8 


Bignonia Catalpa, 246 

Blanchard, W. H., 158 

Blome, W. H., 124 

Boerker’s Our National Forests (Re- 
view), 14 

Book Reviews, 228 

Botanical Abstracts, 230 

Botanical Explorations in 
123 

Botanical Gardens at Buitenzorg, Java, 
The, 34 

Botanical Study of Skunk Cabbage, 
Symplocarpus foetidus, A, 21 

Botany in the City High School, 57 

Brassica sp., I2, 13 

Britton, E. G., 18, 79, 157, 230; The 
Swiss League for the Protection of 
Nature (Review), 101 

Britton, N. L., 103, 158, 159, 203, 231; 
Flora of the District of Columbia 
(Review), 244; Testimonial dinner 
to, 105 

Britton and Rose’s Cactaceae (Re- 
view), 200 

Briza minor, 222 

Broadhurst, J., 19, 82 

Bromus carinatus, 222, 227; Gussoni, 
193; hordeaceus, 103, 222, 227; 
hordeaceus leptostachys, 222; margi- 
natus, 222, 227; polyanthus, 222; 
racemosus commutatus, 193; rubens, 
222; secalinus, 222, 227; sterilis, 
222, 226; tectorum, 222, 227; tec- 
torum nudus, 222; villosus, 222, 
227; vulgaris, 222, 226; vulgaris 
eximius, 222 

Brooklyn Botanic Garden, 20; meeting 
at, 122 

Brown, C., 247 

Bryological Notes—V., Scapania nim- 
bosa from Norway, 49 

Bryum neodamense, 232; 
232 

Buchnera, 113; americana, 235 

‘Buellia geographica, 248 

Bulgaria globosa, 231 

Burnham, S. H., The Sedges of the 
Lake George Flora, 125 

Burns, G. P., 84, 159 

Bursa bursa-pastoris heegeri, 137; heeg- 
eri,I37 


Equador, 


pallescens, 


Calamagrostis lactea, 191; Langsdorfii 
lactea, IOI 

Caldwell, O. W., 104 

Calistachya alba, 161; virginica, 161 

Calopogon pulchellus, 153 


Calvatia gigantea, 248 

Canadian Arctic Mosses, 232 

Cannon, W. A., 51 

Capnorea, 181 

Capraria gratioloides, 149 

Cardot, J., 33 

Carex, 181; albicans, 132; aperta, 125; 
albursina, 133; anceps, 133; arctata, 
133; Asa-Grayi, 136; aurea, 133; 
Baileyi, 136; blanda, 133; Bicknellii, 
132; bromoides, 131; brunnescens, 
I3I; Canescens, 131; castanea, 133; 
cephalophora, 130; cephaloidea, 130; 
chordorrhiza, 129; communis, 132; 
comosa, 136; complanata, 134; com- 
planata robusta, 134; conoidea, 133; 
Crawfordii, 131; crinita, 135; crista- 
tella, 131; cryptolepis, 135; Dewey- 
ana, 131; digitalis, 133; disperma, 


130; eburnea, 132; exilis, 131; fes- 
tucacea, 132; flava, 135; flexuosa, 
133; foenea, 132; folliculata, 135; 


formosa, 133; gracillima, 133; granu- 
laris, 133; grisea, 133; gyandra, 135; 
hirtifolia, 132; Hitchcockiana, 133; 
Houghtonii, 135; hystricina, 136; 
hystricina Dudleyi, 136; intumes- 
cens, 136; lacustris, 136; lanuginosa, 
135; lasiocarpa, 135; laxiculmis, 133; 
laxiflora, 133; Leersii, 131; leersii 
angustata, 131; Leersii cephalantha, 
131; leptalea, 3132; limosa, 134; 
lupulina, 136; lupulina Bellavilla, 
136; lupulina X retrorsa, 136; Jurida, 
136; lurida X lupulina, 136; monile, 
135; Novae-Angliae, 132; normalis, 
131; normalis perlonga, 131; Oedeti, 
125; pallescens, 134; pauciflora, 132; 
paupercula, 134; pedunculata, 132; 
pennsylvanica, 132; plantaginea, 133; 
platyphylla, 133; prairea, 130; pro- 
jecta, I3I; prasina, 133; Pseudo- 
Cyperus, 136; retroflexa, 129; re- 
trorsa, 136; rosea, 129; scabrata, 
134; scoparia, 131; sparganioides, 
130; Sprengelii, 134; squarrosa, 125; 
stipita, 130; straminea, 131; stricta, 
I35; Swanii, 134; tenuiflora, 130; 
trichocarpa, 135; trisperma, 130; 
tribuloides, 131; torta, 135; Tucker- 
mani, 136; umbellata, 132; varia, 
I32; vestita, 135; virescens, 134; 
vulpinoidea, 130; xanthocarpa, 130 

Carnegiea gigantea, 200 

Carpenter, W. H., 105 

Carpolithes macrophyllus a 
delphus, 244 

Cassandra, 153 

Cassiope, 175; tetragona, 18 

Castanea pumila, 9 


Phila- 


252 


Castilleja, 113; coccinea, 236, 240 

Catalpa Catalpa, 246 

Catoscepium nigritum, 232 

Celtis mississippiensis, 9, 10; 
dentalis, Io 

Cenchrus carolinianus, 188 

Centaurea Jacea, 13 

Cercis, I21 

Chamberlain, E. B., 33 

Changes in Teaching Biology in our 
High Schools, 65 


Chelone glabra, 117, 240; glabra 
tomentosa, 117, 240; Penstemon, 
II5 


Chivers, A. H., 103 

Chlonanthes tomentosa, 117 

Chloris radiata, 188 

Chrysanthemum Leucanthemum, 12 

Chrysohypnum stellatum, 232 

Chrysophlyctis endobiotica, 159 

Chrysopsis mariana, 12; villosa, 184 

Cichorium Intybus, 12 

Cinna latifolia, 191; pendula, 191 

Cireaea pacifica, 184 

Cnicus, 181 

Cockayne, A. H., 204 

Cockerell, T. D. A., Carpolithes macro- 
phyllus a Philadelphus, 244; Heli- 
anthus Besseyi Bates, 197; Notes 
on Coelogyne, 227; Notes on Lycasti, 
10; Some Western Columbines, 137 

Coelogyne asperata, 228; cristata, 227; 
pandurata, 227; sparsa, 228; speciosa, 
228 

Cohen, N., 247 

Coker, D., 18 

Collomia, 175 

Columbia University, Meeting at, 79 

Conarum, 175 

Comparison of the Flora of Southern 


British Columbia with that of the - 


State of Washington, as Illustrated 
by the Floras of Henry and Piper, 
174 

Concerning Duplicate Types, 13 

Conobea borealis, 146 

Cooper, W. S., 83 

Corallorrhiza odontorhiza, 153 

Correction, A, 83 

Corvus Corvus, 246 

Corylus californica, 183 

Cupressus Macnabiana, 92; nevadensis, 
92; Sargenti, 92 

Cynodon Dactylon, 188 

Cynosurus, 180; cristatus, 
echinatus, 189 

Cyperus dentatus, 126; diandrus, 126; 
esculentus, 126; filiculmis, 126; 
Houghtoni, 126; inflexus, 126; rivu- 
laris, 126; strigosus, 126 


189, 221; 


occi- . 


Cypripedium arietinum, 153, 155; parvi- 
flora, 182 
Cytisus scoparius, 184 


Dactylis glomerata, 223, 227 

Damon, W. E., 103 

Danthonia americana, 221, 226; cali- 
fornica, 221 

Dasiphora, 175 , 

Dasystephana Menzesii, 49; spathacea, 
49 

Dasystoma virginica, 49 

Daucus carota, 12 

DeForest, R., 105 


Denslow, H. M., Reminiscences of 
orchid-hunting, 152 

Deschampsia casepitosa, 221, 226; 
calycina, 191; danthonioides, 221; 


elongata, 221; holciformis, 189 
Dianthus, 180; Armeria, 13 
Dicostegia, 3 
Dicranum elongatum, 232 
Digitaria humifusa, 188, 219, 226 
Dipsacus, T8t 
Distichlis maritima, 192 
Distribution of the Montane Plants of 
the Rocky Mountains, The, 34 
Dodge, B. O., 19, 248; Proceedings of 


the) (Club; 17,918) 10; sem OumsOes 
WA, Wisp, Bali] 

Douglass, H. B., 247 

Drepanocladus aduncus, 232; brevi- 


folius, 232; scoprioides, 232 
Dryas integrifolia, 18 
Drymocallis, 175 
Duggar, B. M., 124 
Dulichium arundinaceum, 129 


Eatonia obtusata, 192; pennsylvanica, 
192 

Echinochloa -Crus-galli, 219 

Ecological Society of America, 84 

Elatine, 181 

Eleocharis acicularis, 127; acuminata, 
127; capitata, 246; diandra, 126; 
intermedia, 127; obtusa, 126; oliva- 
cea, 126; palustris, 127; tenuis, 127, 


246 
Eleusine tristachya, 188 
Elymus dasystachys, 1090; glaucus, 


225, 226; littoralis, 193; mollis, 103; 
saxicolus, 193 ‘ 
Encalypta brevicola, 232 


‘Ephedra viridis, 92 


Eragrostis cyperoides, 189; hypnoides, 
221, 226; Orcuttiana, 189; reptans, 
192 

Erigeron, 181; canadensis, 13; filiformis, 
183; ramosus, 13 

Eriocaulon septangulare, 13 


Eriogonum, 181 

Eriophorum alpinum, 127; callithrix, 
127; gracile, 127; virginicum, 127; 
viridicarinatum, 127 

Erythronium albidum, 43; americanum, 
43; propullans, 43-47 

Eucapholus, 175 

Euchroma coccinea, 236 

Eupodium, 3 

Eustachya alba, 161 

Evans, A. W., 18, 19, 81; A New Riccia 
from Peru, 85 

Exhibition of a Collection of Flowering 
Plants and Mosses from North Star 
Bay, 18 


Farlow, W. G., 142 

Farwell, O. A., 124 

Ferguson, W. C., Plants in Flower in 
the Autumn of 1918 on Long Island, 
BV, tE2 

Festuca brevifolia, 192; bromoides, 189, 
223; californica, 192, 223; denticu- 
lata, 192; elatior, 224, 227; hetero- 
phylla, 189; idahoensis, 224, 226; 
Jonesii, 192; microstachys, 192; mega- 

“Jura, 189, 223, 226; myuros, 223; 
occidentalis, 224, 226; octoflora, 223, 
226; ovina, 192; ovina columbiana, 
192; ovina ingrata, I92; ovina ore- 


gana, 193; rubra, 223, 226; rubra 
littoralis, 193; rubra megastachys, 
189, 224; rubra pubescens, 193; 


scabrella, 193; subulata, 224, 226 
Fimbristylis autumnalis, 127 
Flora of the District of Columbia (Re- 
view), 244 — 
Frasera, 181 


Gager, C. S., 19, 81, 104, 122; Boerker’s 
Our National Forests (Review), 14; 
Macfarlane’s The Causes and Course 
of Organic Evolution (Review), 93 

Gastridium australe, 191 

Garrett, O. A., 185 

Gentiana Menzesii, 
49 

Gilia, 175 

Gleason, H. A., 34, 36, 53, 203; Rham- 
nus dahurica in Michigan, 141; 
What is Ecology? 89 

Globifera micranthemoides, 150 

Gluck, M., 247 

Glycena grandis, 225, 226; leptostachya, 
224, 226; -occidentalis, 224, 226; 
pauciflora, 224, 226 

Gnaphalium obtusifolium, 13 

Goodlatte, A., 231 

Goodyeara pubescens, 153 

Gratiola anagallidea, 150; aurea, 144, 


49; spathacea, 


145, 240; aurea obtusa, 144, 145, 240; 
dubia, 149; inaequalis, 149; neglecta, 
144, 146, 147, 240; pilosa, 144, 240; 
sphaerocarpa, 147; virginiana, 144, 
146, 147, 240; viscidula, 144, 145; 
viscosa, 145 

Grasses of Salem, Oregon and Vicinity, 
The, 216 

Graves, H. S., 20 

Gundersen, A., Trelease’s Plant Mate- 
rials and Winter Botany (Review), 
78 

Gymnotheca, 3 

Gynerium argenteum, 221 


Habenaria, 175; ciliaris, 153; Hookeri, 
154, 155; macrophylla, 154; orbicu- 
lata, I 

Hankinson, T. L., 159 

Harper, R. A.,. 18, 79, 83, 103, 104, 
105, 157, 158, 231, 247 

Harper, R. M., The Supposed Southern 
Limit of the Eastern Hemlock, 
198; Tumion taxifolium in Georgia, 
119 

Harrimanella, 175 

Harris, J. A., 19, 82 

Harvey, R. B., 122 

Harwood’s New Creations 
Life (Review), 15 

Hazen, T. E., 247 

Helenium tenuifolium, 37 

Helianthus alexanderi, 197; apricus, 198; 
apricus camporum, 198; nebrascensis, 
197; nitidus, 198; tuberosus, 197 

Helianthus Besseyi Bates, 197 

Hemianthus, 111, 150 micranthemoides, 
I50; micranthus, 150, 240 

Hemicarpha, 181 

Hieracium scabrum, 13 

Hierochloe macrophylla, 220, 226 

Hitchcock, A. S., 185 

Holcus lanatus, 192 

Hollick, A., 105 

Hopkins, L. S., The Occurrence and 
Distribution of Vasey’s Pondweed in 
Northeastern Ohio, 243 

Hordeum Gussoneanum, 225; jubatum, 
225; maritimum, 193; murinum, 
225, 227; nodosum, 225 

Horkelia, 181 

Houstonia longifolia, 12 

Hovey, E. O., 18 

Howe, M. A., 19, 79, 81, 81, 142, 157, 
158, 231, 247; Proceedings of the 
Club, 230 

Hughes, F. T., 104; Botany in the City 
High Schools, 57 


in Plant 


Ichnanthus, 51 


254 


Ilex opaca, I21 

Ilysanthes, Ill, 148; dubia, 148, 149, 
240; dubia inundata, 149, 241; 
gratioloides, 149; inaequalis, 140, 
241; riparia, 148 

In the Wake of the Enemy, 32 

Ionactis linariifolius, 13 

Isotria verticillata, 153, 155 


Japanese Honeysuckle in the Eastern 
United States, The, 37 

Johnson, D. S., 158 

Johnston, D. W., 247 

Journal of the International Garden 
Club, 204 

Journal of the New York Botanical 
Garden, 19 

Jurica, H. S., 247 


Knight, L. T., 20 

King, C. A., 104; Changes in Teaching 
Biology in Our High Schools, 65 

Kimball, K. D., 51 

Kirkwood, J. E., 17 

Kleinsmid, R. B., von, 34 

Knight, L. T., 20 

Kobbe, F., 247 

Koeleria cristata, 222 

Kunkel, L. O., 80 


Lasiacis anomala, 51 

Leersia oryzoides, 219, 226 

Leon, Bro., A New Cuban Sida, 172 

Leptandra, 161; virginica, 161 

Leptobryum pyriforme, 232 

Lepturus incurvatus, 189 

Levin, I., 158 

Levine, M., 19, 82, 83 

Limnanthemum Grayanum, 48 

Limnanthes, 180 

Limnorchis, 175 

Limosella aquatica, 30, 3I, 143; mari- 
tima, 143; subulata, 30, 31, 32, 143, 
241; tenuifolia, 30 

Limosella, Some Remarks upon, 30 

Linaria canadensis, 151, 241; Linaria, 
I2, I5I, 241; pennsylvanica, 151; 
vulgaris I51 

Liparis liliifolia, 153, 155 

Liquidambar, 121 

Liriodendron, 121 


Lisk, H., 80 
Listera, 156; convallarioides, 154; cor- 
data, 154 


Lobelia, 175 


Lolium multiflorum, 189, 224, 227; 
perenne, 189, 224, 227; perenne 
cristatum, 225, temulentum, 224, 
227 


Lomatium, 181 


Lonicera japonica, 37 

Lupinus, 181 

Lurvey, S. A., 79, 80 

Lycaste alba, 11; cruenta, 11; Skinneri, 
Io, 11; Skinneri alba, 10 

Lysichiton Kamtschatcensis, 21, 183 

Lysimachia terrestris, 246 


MacCaughey, V., The Pala or Mule’s- 
foot Fern (Marattia Douglasii (Presl.) 
Baker) in the Hawaiian Archipelago, 
I 

MacDougal, D. T., 105 

Macfarlane’s The Causes and Course 
of Organic Evolution (Review), 93 

Machoeranthera, 175 

Madronella, 181 

Magnolia grandiflora, 121 


Mann, P. B., 104; The Relation of 
First Year Botany to Advanced 
Work, with References to Certain 


Applications and By-products, 72 

Marattia alata, 3; attenuata, 3; Boivini, 
3; circutifolia, 3; Douglasii, 1-8; 
fraxinea, 3; Kaulfussii, 3; levis, 3; 
melanesiaca, 3; pellucida, 3; pur- 
purascens, 3; salicina, 3; salicifolia, 
(3; sambucina, 3; Weinmanniifolia, 
3 

Mariscus mariscoides, 129 

MeNeier, E., 247 

Medicago, arabica, 183 

Melampyrum, 114; americanum, 238, 
239; americanum latifolium, 238; 
cristatum, 238; latifolium, 238; line- 
are, 238,. 241; lineare americanum, 
239; lineare latifolium, 238 239; 
pratense americanum, 238 

Melica acuminata, 192; bromoides, 
192; bulbosa, 192; Geyerl, 222; 
Harfodii, 192; interrupta, 190; scabra- 
ta, 192; subulata, 222, 226 

Melilotus alba, 12, 13 

Micranthemum micranthemoides, 150; 
micranthum, 150; Nuttallii, 150 

Microseris, 175 

Mimulus, ri, 147; alatus, 147, 148, 
241; guttatus, 147, 148; moschatus, 
147; ringens, 147, 148, 241 

Mnium affine, 232 

Moore, B., 20, 84, 159 

Moore, G. T., 105 

Morphogenesis in Dictyostelium, 231 


‘Mucor, 18 


Murrill, W. A., 105 
Mycosphaerella, 18 
Myosurus minimus, 183 
Myriotheca, 3 


Nabalus sp., 13 


255 


Nash, G. V., 203 

Nassella chilensis, 188 

Navarretia, 175 

Nelson, J. C., A Comparison of the 
Flora of Western British Columbia 
with that of the State of Washing- 
ton, as Illustrated by the Floras 
of Henry and Piper, 174; The Grasses 
of Salem, Oregon and _ Vicinity, 
216; Notes on the Grasses of Howell's 
Flora of Northwest America, 187 

Neopieris mariana, 12 

Neoplastic Diseases (Cancer) in the 
Animal and Vegetable Kingdoms, 
158 

New California Cypress, A. Cupressus 
nevadensis sp. nov., 92 

New Cuban Sida, A., 172 

Newcombe, F. C., 20 

New Names for Species of Phanerogams, 
48 

New Riccia from Peru, A, 85 

News Items, 19, 36, 83, 105, 124, 142, 
158. 185, 203 

New York Botanical Garden, 51, 203; 
Meetings at, 17, 33, 82, 103, 157, 230 

New York Evening Sun, 36 

Nishimura, M., 17 

North American Flora, 36 

Nichols, G. E., 18, 19, 34, 82 

Notes and News, 51 

Notes on Coelogyne, 227 

Notes on Lycaste, 10 

Notes on Grasses of Howell’s Flora 
of Northwest America, 187 

Notholcus lanatus, 220, 227 

Nymphoides Grayanam, 48 


Occurrence and Distribution of Vasey’s 


Pondweed in Northeastern Ohio, 
243 , 
Oenothera, 175; biennis, 12, 245; 


muricata, 13 

Olive, E. W., 20, 83, 102 

Onagra, 175 

Onobrychis sativa, 183 

Opuntia, 200, 201; ficus-indica, 202; 
tuna, 201; vulgaris, 201 

Orchis spectabilis, 155 

Orobanche, 175 

Oryzopsis cuspidata, I91 

Osborn, 105 

Osmuda sp., 9; spectabilis, 9 

Osterhout, G. E., 79, 80 

Ostrya, I21 

Otophylla, 113; auriculata, 215; 241; 
Michauxii, 216 

Owen, T., 17 

Oxycoccus, 175 - 


Pachylophus, 1811 

Pala or Mule’s-foot Fern (Marattia 
Douglasii (Presl.) Baker) in the 
Hawaiian Archipelago, The, 1 

Panicularia fluitans, 190; nervata, 192; 
occidentalis, 189 


Panicum amalurum, 51; barbinode, 
188; barbipulvinatum, 219, 226; 
capillare, 190 219; crus-galli, 190; 
dichotomum, 190; miliaceum, 188, 


219; pacificum, 188, 219, 226; pubes- 
cens, 190; prutiens, 483; sanguinale, 
48, 190; scoparium, 190; Scribneria- 


num, 219, 226; thermale, 188; 
urvilleanum, 51 

Papaver radicatum, 18; somniferum, 
182, 183 

Parrya, 181f 

Paspalum dilatatum, 188; distichum, 
219, 226 

Pediculatis, 114; auriculata, 237; cana- 
densis, 237, 241; gladiata, 237; 


lanceolata, 237, 241; palustris, 236; 
pallida, 237 

Pellia epiphylla, 88; Neesiana, 88 

Pennell, F. W., 20, 80, 81, 83, 157, 158, .- 
231; Concerning Duplicate Types, 
13; Scrophulariaceae of the Local 
Flora—I, 107;—II, 143;—III, 161; 
—IV, 205;—V, 235; Some Remarks 
upon Limosella, 30 

Pen temon, I10, I15, 181; digitalis, 
TLIO; 240 hirsutus, LO, LZ; 24E; 
pallidus, 116, 241; Pentstemon, 116; 
tubiflorus, 115, 116 

Pereskia, 200 

Persicaria pennsylvanica, 13 

Phalaris arundinacea, 219; brachy- 
stachys, 188; canariensis, 219; minor, 
188; paradoxa, 188 

Phegopteris phegopteris, 182 

Philadelphus Lewesii, 182; 
phyllus, 244 

Phleum pratense, 220, 227 

Phragmites communis, 224, 226 

Phyllodoce glanduliflorus, 182 

Pinus glabra, 121; monophylla, 92; 
palustris, 199; Taeda, 121 

Piperia, 175 

Plantago aristata, 13; lanceolata, 13 

Planting of Trees as War Memorials, 34 

Plants in Flower in the Autumn of 
1918 on Long Island, N. Y., 12 

Pleistocene Plants from Tennessee n 
Mississippi, 8 

Pleuropogon, refractus, 222, 226 

Poa alcea, 189; annua, 223, 
Buckleyana, 191; compressa, 
226; flava, 192; Fendler ana, 
glauca, 190; Howellii, 223, 


macro- 


227; 
223, 
182; 
226; 


256 


incurva, 192; invaginata 192; lep- 
tocoma, 223, 226; multnomae, 223; 
nervosa, 223, 226; occidentalis, 192; 
pratensis, 223, 227; purpurascens, 
192; reflexa, 192; scabrella, 192, 223, 
226; triflora, 223, 226; trivialis, 189, 
223, 227 , 

Pogonia ophioglossoides, 153 

Polygonella articulata, 13 

Polygonum minimum, 183; 
183 

Polypogen monspeliensis, 220 

Potamogeton Vaseyi, 243 

Potentilla, 175, 181 

Prickly Pears of the Southeastern 
United States, The, 103 

Primula, 180 

Proceedings of the Club, 17, 33, 79, 
LO2Q) T2257 220 247 

Prunella vulgaris, 12 

Pseudotsuga taxifolia, 218 

Ptilocalais, 175 

Puccinellia angustata, 
cula, 189 

Puccinia Andropogonis, 49; Gentianae, 
49; oahuensis, 48; Scirpi, 48; sub- 
striata, 48 


Nuttallii, 


183; pauper- 


Quercus alba, pagodaefolia, 9; 


predigitata, 9 


DL 


Ranunculus, 175, 181; nivalis, 18 

Rapuntium, 175 

Relation of First Year Botany to Ad- 
vanced Work, with Reference to 
Certain Applications and By-prod- 
ucts, The, 72 

Reminiscences of Orchid-hunting, 152 

Reviews, 14, 78, 93, 122, 200, 228, 244 

Rhamnus dahurica in Michigan, 141 

Rhinanthus, 113; coccinea, 236; Crista- 
galli, 236; virginicus, 49 

Rhynchospora alba, 129; capillacea, 
129; fusa, 129; glomerata, 129 

Rhytidium rugosum, 232 

Riccia bistriata, 85 

Richards, H. M., 10, 34, 79, 81, 82, 102, 
I04, 123, 158, 248 

Rock rH. es 


Rock’s Lobelioideae of Hawaii (Re- 
view), 228 

Roosevelt’s Notes on Brazijian Trees, 
194 

Rose, J. N., 123, 159 

Rosendahl, C. O., Variations in the 


Flowers of Erythronium propullans 
Gray, 43 

Rubus sp., 13 

Rudbeckia hirta, 13 

Runge, A. G., 79, 80 


Rusby, H. H., 53 
Rydberg, P. A., 34 


Sagina occidentalis, 183 

Salix, 181; groenlandica, 18; herbacea, 
18 

Salsola pestifer, 37; rhombifolia, 37; 
spinosa, 37 

Sanguinale pruriens, 48 

Saxifraga, 181; oppositifolia, 18 

Sassafras Sassafras, 246 

Science, 20 

Scapania nimbosa, 49, 50; ornithopodi- 
oides, 49; planifolia, 49, 50 

Schizonotus, 175 

Schneider, C., 53, 185 

Schwalbea, 113; americana, 235, 241 

Scirpus americanus, 128; atrovirens, 
128; atrocinctus, 129; cyperinus, 129; 
debilis, 128; fluviatilis, 128; lineatus, 
128; microcarpus, 128 occidentalis, 
128; Peckii, 128; pedicellatus, 1209; 
polyphyllus, 128; Smithii, 128; sub- 
terminalis, 128; sylvaticus, 128; Tor- 
eyi, 128; validus, 128 

Scleropoa 1tigida, 189, 224 

Scott, J. G., 80 

Scrophularia, 110, 117; lanceolata, 119; 
leoprella, 118, 241; marilandica, 118, 
241; nodosa, 117; nodosa lanceolata, 
I19; nodosa marilandica, 119 

Scrophulariaceae of the Local Flora, 
TO7, LASw LOL 2058235 

Seaver, F. J., 18, 79, 231, 247 

Sedges of the Lake George Flora, The, 
125 

Sedum, 175; rosea, 182 

Selaginella apus, 105 

Senites Hartwegi, 48 

Senicio, 181 

Setaria imberbis, 188; viridis, 219 

Seymore, A. B., 142. 

Shantz, H: L., 84 

Shorter Notes, 141, 197, 244 

Sida Brittoni, 172; ciliaris, 173 

Sieversia, 175 

Singewald, J. T., 19 

Sisyrhynchium bermudiana, 157 

Sitanion, 181; Brodiei, 193; elymoides, 


I93; flexuosum, 1093; glaber, 1093; 
Hystrix 193; jubatum, 1093, 225; 
Leckenbyi, 193; planifolium, 103; 


rigidum, 193; villosum, 193 


. Skottsberg, C., 185 


Small, J. K., 103 

Smith, C3 Ps 

Smith, J. D., 158 

Solidago bicolor, 13; caesia, 13; juncea, 
12, 13; nemoralis, 13; puberula, 13; 
rugosa, 13 


257 


Some Plant Diseases Survey Work in 
New York, Virginia and Pennsyl- 
vania, 102 

Some Remarks upon Limosella, 30 

Some Western Columbines, 137 

Sophramanthe pilosa, 145 

Spartina cynosuroides, 191 

Sphaerostigma, 181 

Sphagnum Moss and its Use in Surgical 
Dressings, 18 

Spiraea, 175 

Spiranthes cernua, 153; gracilis, 153 

Sporobolus Bolanderi, 190; cuspidatus, 
190; depauperatus, 190; gracillimu«, 


190; filiformis, 190; indicus, 172; 
simplex, 190 
Standley, P. C., 185 
Stenophyllus capillaris, 127 
Stipa Bloomeri, 1091; Kingii, 191; 


Lemmoni 220, 226; Lemmoni Jonesii, 
188; littoralis, 188; Michauxiana, 
I9I; minor, I91; oregonensis, I91; 
occidentalis, 191; viridua, 191 

rout, A. B., 19, 82, 232 

Supposed Southern Limit of the Eastern 
Hemlock, The, 198 

Swartzia montana, 232 

Swiss League for the Protection of 
Nature (Review), ror 

Symplocarpus foetidus, 21 

Symposium and Conference on Botan- 
ical Education in the Secondary 
Schools, 104 

Syntherisma, 181; pruriens, 83 


Taraxacum Taraxacum, 12 

Taraxia, 181 

Taubenhaus, J. J., 36 

Taxus floridana, 120 

Taylor, N., 19, 79, 80, 81, 82 84, 159; 
Britton and Rose’s Cactaceae (Re- 
view), 200; Rock’s Lobelioideae of 
Hawaii (Review), 228; Roosevelt’s 
Notes on Brazilian Trees, 194 

Taylor, Rose M., death of, 36 

Thalesia, 175 

Theriot, M., 133 

Thermopsis, 181 

Thompson, W. G., 105 

Tonella, 181 

Torreya taxifolia, 119 

Trees of France, The, 32 

Trelease’s Plant Materials and Winter 
Botany (Review), 78 

Trias oblonga, 227 

Trichostema, 181 

Trifolium agrarium, 13; arvense, 13, 
I2; pratense, I2, 13; repens, 12, 13 


Trisetum barbatum, 
221, 226; cernuum, 
spicatum, Ig1 

Triticum vulage, 225, 227 

Tsuga canadensis, 198, 199 

Tumion taxifolium in Georgia, 119 

Types of Sterility in the Radish, 232 


TOT, 
221, 


canescens, 
226; sub- 


Uredo zeugites, 48 


Vaccinium, 153, 175 

Valerianella salmonifolia, 184 

Vancouveria hexandra, 183 

Variations in the Flowers of Erythron- 
ium propullans Gray, 43 

Verbascum, 109, 114; blattaria, 114, 
II5, 241; lychnitis, 114, I15, 241; 
phlomoides, 114, 115; Thapsus, 115, 
PAT. TS 

Veronica, I12, 162; agrestis, 162, 165; 
americana, 164, 167, 169, 241; 
Anagallis latifolia, 168; arvensis, 163, 
167, 241; Beccabunga, 169; Brit- 
tonii, 165, 168, 242; Chamaedrys, 
164, 167, 242; diffusa, 165; glandi- 


fera, 165, 170, 242; hederaefolia, 
162, 165; humifusa, 166; longifolia, 
164, 167; neglecta, 166; officinalis, 
164, 167; 242; peregrina, 242; 163, 


167, 242; peregrina xalapensis, 164, 
167; precox, 165; ruderalis, 163, 
166; scutellata, 165, I7I, 242; serpyl- 
lifolia, 163, 165, 166, 242; Teucrium, 
164, 167; Tournefortii, 163, 165, 
242; virginica, 161; xalapensis, 167 

Veronicastrum, I12, 161; album, 161; 
virginicum, I61, 242 

Victorin, Bro. M., 34 

Vinca, 180 

Viola, 181; pedata, 13 


What is Ecology?, 89 

White, O. E. Harwood’s New Creations 
in Plant Life (Review), 15 

Whitford, H. N., 142 

Williams, K. A. A Botanical Study 
of Skunk Cabbage, Symplocarpus 
foetidus 21 

Williams, R. S., 18, 232 

Wilson, E. H., 105 

Wilson, McL., The Trees of France, 32 

Wilson, P., 79 

Woodward, R. W., 103 


Xanthium canadense, 182 


Zea Mays, 225 
Zengites Hartwegi, 48 


ak 


it ol ies 


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Committees for 1919. 


Finance Committee Program Committee 
R. A. HARPER, Chairman. Mrs. E. G. Britton, Chairman. 
- ‘J. H. BARNHART, PROF. JEAN BROADHURST 
"Miss C. C. HayNEs B. O. DopGE 
'SERENO STETSON MICHAEL LEVINE 


F. J. SEAVER 


Budget Committee 
Membership Committee 


J. H. BARNHART, Chairman. 


R. A. HARPER J. K. SMALL, Chairman. 

N. L. BRITTON T. E, HAZEN 

A. W. EVANS E. W. OLIVE 

M. A. Howe : : 

H. H. Ruspy Local Flora Committee 


N. L. Britton, Chairman. 


Field Committee ae ¢ 
F. W. PENNELL, Chairman. eEeants: FyptOname; 


Mrs. L. M. KEELER E. P. BICKNELL Mrs. E.G. BRITTON 
MICHAEL LEVINE N. L. BRITTON T. E. HAZEN 
GEORGE T. HASTINGS C. C. Curtis M. A. Howe 

PEercy WILSON _K. K. MACKENZIE MICHAEL LEVINE 
F. J. SEAVER NoRMAN TAYLOR W.A. MurRRILL 


Chairmen of Special Committees on Local Flora 
Ferns and Fern Allies: R. C. Benedict. Lichens: W. C. Barbour 


Mosses: Mrs. E. G. Britton Sphaeriaceae, Dothideaceae: H. M 
Liverworts: A. W. Evans Richards } 
Fresh Water Algae: T. E. Hazen Hypocreaceae, Perisporieae, Plectas- 
Marine Algae: M. A. Howe : cineae, Tuberineae: F. J. Seaver 
Gasteromycetes: G. C, Fisher Fungi-forming sclerotia: A. B. Stout 
Hymenomycetes: W. A. Murrill Imperfecti: H. M. Richards, F. 
Except Russula and Lactarius: Miss G. Seaver, Mel T. Cook 
Burlingham Oomycetes: C. A. King 
Cortinarius: R. A. Harper Zygomycetes: A. F. Blakeslee 
Polyporeae: M. Levine Chytridiaceae, 
’ Exobasidii: H, M. Richards Myxomycetes: Mrs. H. M. Richards 
Rusts and Smuts: E. W. Olive .. Yeast and Bacteria: Prof. J. Broadhurst 


Discomycetes: B.O. Dodge © Insect galls; Mel T. Cook 


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addressed to 
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